S-furfuryl thioformate
2-furanmethanethiolformate
 
Notes:
Flavouring ingredient
  • BOC Sciences
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      59020-90-5 2-Furanmethanethiol formate 98.0%
       
  • Endeavour Specialty Chemicals
    • Endeavour Specialty Chemicals Ltd
      Expertise in high impact aroma chemicals
      Endeavour Speciality Chemicals offers high-impact aroma chemicals, at small to medium scale.
      Speciality Chemical has more than 25 years experience of manufacturing high-impact aroma chemicals. With our core expertise in sulfur and heterocyclic chemistries, Endeavours products have applications in a range of industry sectors including flavours and fragrances, pharmaceutical research and material sciences. Endeavour also offer custom synthesis and contract manufacturing services at their UK manufacturing site.
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      TE0170 2-Furanmethanethiol formate
       
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    • M&U International LLC
      Steady supply & demand
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      H0156 FURFURYL THIOFORMATE, Kosher
       
  • Penta International
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      Product(s):
      06-26500 2-FURANMETHANETHIOL FORMATE
       
  • Robinson Brothers
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  • Sunaux International
    • Sunaux International
      Buy With Confidence
      We have industry leading processes and procedures to ensure nothing but the most reliable product.
      Sunaux International was founded in 2012 by the owner Mr.John Felton after spending 18 years involved in developing global business in the aromatic chemicals, fragrance and flavour compounds business.
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      H0156 Furfuryl Thioformate
       
  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
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      Product(s):
      W0475 2-Furanmethanethiol Formate
       
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    • TCI AMERICA
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      F0688 S-Furfuryl Thioformate >95.0%(GC)
       
  • R C Treatt & Co Ltd
    • R C Treatt and Co Ltd
      Innovative ingredient solutions
      World-leading innovative ingredient solutions provider for the flavour, fragrance and FMCG industries.
      We offer innovative and trend-setting product concepts for our customers, collaborating with them to create true value for their products.
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      2-Furanmethanethiol formate Halal, Kosher

      Used in coffee, meat and nut flavours, for meat products at 1ppm, bakery and soft/frozen confectionery at 0.5ppm, and desserts at 0.2ppm.
       
       
  • United International
    • Qingdao Free Trade Zone United International Co Ltd
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      Qingdao Free Trade Zone United International Trade Co., Ltd.was founded in 1996, specializing in the production and import and export of food additives,flavor raw materials and pharmaceutical and chemical raw materials. The company has experienced R&D and business personnel,product quality, low price, efficient service and fast insight and grasp the latest market information.
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      9016 Furfuryl Thioformate
       
Synonyms   Articles   Notes   Search
CAS Number: 59020-90-5Picture of molecule3D/inchi
FDA UNII: JK1M930RJC
Nikkaji Web: J308.593G
MDL: MFCD00209507
CoE Number: 11770
XlogP3-AA: 1.30 (est)
Molecular Weight: 142.17722000
Formula: C6 H6 O2 S
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: Register name to be changed to: S-Furfuryl thioformate.
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
JECFA Food Flavoring: 1073  S-furfuryl thioformate
FLAVIS Number: 13.051 (Old)
DG SANTE Food Flavourings: 13.051  S-furfuryl thioformate
FEMA Number: 3158  S-furfuryl thioformate
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):59020-90-5 ; 2-FURANMETHANETHIOL FORMATE
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to yellow brown clear liquid (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.21300 to 1.22300 @  20.00 °C.
Pounds per Gallon - (est).: 10.105 to 10.188
Refractive Index: 1.53900 to 1.54900 @  20.00 °C.
Boiling Point: 66.00 °C. @ 15.00 mm Hg
Boiling Point: 80.00 to  87.00 °C. @ 10.00 mm Hg
Vapor Pressure: 0.102000 mmHg @ 25.00 °C. (est)
Flash Point: > 230.00 °F. TCC ( > 110.00 °C. )
logP (o/w): 1.051 (est)
Soluble in:
 alcohol
 water, 5723 mg/L @ 25 °C (est)
Insoluble in:
 water
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Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: sulfurous
 
Odor Strength: high ,
recommend smelling in a 0.10 % solution or less
 
 sulfurous  coffee  nutty  
Odor Description:
at 0.10 % in dipropylene glycol. 
sulfurous coffee nutty
 
 
Flavor Type: sulfurous
 
 coffee  
Taste Description:
coffee
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
Synonyms   Articles   Notes   Search   Top
Suppliers:
Ambles Nature et Chimie
FURFURYL THIOFORMATE
BOC Sciences
For experimental / research use only.
2-Furanmethanethiol formate 98.0%
Endeavour Specialty Chemicals
2-Furanmethanethiol formate
Speciality Chemical Product Groups
Jinan Enlighten Chemical Technology(Wutong Aroma )
S-Furfuryl thioformate Kosherk
Kingchem Laboratories
FURFURYL THIOFORMATE (2-Furanmethanethiol formate)
M&U International
FURFURYL THIOFORMATE, Kosher
Penta International
2-FURANMETHANETHIOL FORMATE
R C Treatt & Co Ltd
2-Furanmethanethiol formate
Halal, Kosher
Odor: coffee
Flavor: coffee
Used in coffee, meat and nut flavours, for meat products at 1ppm, bakery and soft/frozen confectionery at 0.5ppm, and desserts at 0.2ppm.
Robinson Brothers
2-Furanmethanethiol formate
https://www.robinsonbrothers.uk/chemistry-competences
Santa Cruz Biotechnology
For experimental / research use only.
S-Furfuryl Thioformate
Sigma-Aldrich
2-Furanmethanethiol formate, ≥97%, FG
Odor: butterscotch; horseradish; tropical; ethereal; coffee; wine-like
Certified Food Grade Products
Sunaux International
Furfuryl Thioformate
Synerzine
2-Furanmethanethiol Formate
TCI AMERICA
For experimental / research use only.
S-Furfuryl Thioformate >95.0%(GC)
Tengzhou Jitian Aroma Chemiclal
S-Furfuryl Thioformate
Tengzhou Xiang Yuan Aroma Chemicals
Furfuryl Thioformate
United International
Furfuryl Thioformate
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for S-furfuryl thioformate usage levels up to:
  0.0200 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 1.30 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.02 (μg/capita/day)
NOEL (No Observed Effect Level): 0.83 (mg/kg bw per day)
Structure Class: III
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 4
Click here to view publication 4
 average usual ppmaverage maximum ppm
baked goods: --
beverages(nonalcoholic): -1.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -1.00000
fruit ices: -1.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -1.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Athority(efsa): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 13 (FGE.13); Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14 (Commission Regulation (EC) No 1565/2000 of 18
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 13Rev1: Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14
View page or View pdf
Consideration of sulfur-substituted furan derivatives used as flavouring agents evaluated by JECFA (59th meeting) structurally related to a subgroup of substances within the group of “Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14” evaluated by EFSA in FGE.13Rev1 (2009)
View page or View pdf
Flavouring Group Evaluation 67 (FGE.67): Consideration of 40 furan-substituted aliphatic hydrocarbons, alcohols, aldehydes, ketones, carboxylic acids and related esters, sulfides, disulfides and ethers evaluated by JECFA at the 65th meeting (JECFA, 2006b) and re-evaluated at the 69th meeting (JECFA, 2009c)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 67, Revision 1 (FGE.67Rev.1): Consideration of 40 furan-substituted aliphatic hydrocarbons, alcohols, aldehydes, ketones, carboxylic acids and related esters, sulfides, disulfides and ethers evaluated by JECFA at the 65th meeting (JECFA, 2006b) and re-evaluated at the 69th meeting (JECFA, 2009c)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 65, Revision 1 (FGE.65Rev1): Consideration of sulfur-substituted furan derivatives used as flavouring agents evaluated by JECFA (59th meeting) structurally related to a subgroup of substances within the group of ‘Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14’ evaluated by EFSA in FGE.13Rev2 (2011)
View page or View pdf
EPI System: View
EPA Substance Registry Services (TSCA): 59020-90-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 62144
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 S-(furan-2-ylmethyl) methanethioate
Chemidplus: 0059020905
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References:
 S-(furan-2-ylmethyl) methanethioate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 59020-90-5
Pubchem (cid): 62144
Pubchem (sid): 135019981
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS): View
HMDB (The Human Metabolome Database): HMDB37731
FooDB: FDB016861
Export Tariff Code: 2932.19.1000
ChemSpider: View
EFSA Update of results on the monitoring of furan levels in food: Read Report
EFSA Previous report: Results on the monitoring of furan levels in food: Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food: Read Report
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 chicory root 
3,6-dimethyl pyrazine-2-thiol 
2,5-dimethyl-3-furfurylthio-pyrazine 
2,5-dimethyl-3,6-diethyl pyrazine 
2,6-dimethyl-gamma-thiopyrone 
2,6-dimethyl-thio-gamma-pyrone 
2-hydroxymethyl-6-methyl-pyridine 
4-hydroxymethyl-pyridine 
2-methyl-3-pentyl pyrazine 
2-pentenyl furan 
2-(1-propenyl) pyridine 
2-(thienyl-2)-ethanethiol 
2,3,5-trimethyl phenolFR
 methyl furfuryl disulfideFL/FR
balsamic
2-acetyl furanFL/FR
burnt
2-ethyl-3,5(or 6)-dimethyl pyrazineFL/FR
 coffee dioneFL/FR
 cycloteneFL/FR
 fenugreek absoluteFL/FR
 fenugreek oleoresinFL/FR
isopropenyl pyrazineFL/FR
chocolate
 cocoa hexenalFL/FR
2,6-dimethyl pyrazineFL/FR
2-methyl butyraldehydeFL/FR
2,4,5-trimethyl thiazoleFL/FR
coffee
 cichorium intybus root extractFL/FR
 cichorium intybus root solid extractFL/FR
 coffea arabica seed extractFL/FR
roasted coffea arabica seed extractFL/FR
 coffea arabica seed oilFL/FR
 coffee absoluteFL/FR
arabica coffee bean butterFL/FR
roasted arabica coffee bean essenceFL/FR
roasted coffee bean extractFL/FR
roasted arabica coffee bean oilFL/FR
roasted arabica coffee bean oil CO2 extractFL/FR
 coffee bean oil extractFL/FR
 coffee difuranFL/FR
 coffee resinoidFL/FR
 furfuryl mercaptanFL/FR
1-hydroxy-2-butanoneFL/FR
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
 nutty pyrazineFL/FR
 tropical thiazoleFL/FR
herbal
 thymyl methyl etherFL/FR
medicinal
2,6-xylenolFL/FR
 menthofuranFL/FR
3,5-cocoa pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
4,5-dimethyl-2-ethyl-3-thiazolineFL/FR
2-ethyl-4-methyl thiazoleFL/FR
 filbert heptenoneFL/FR
2,6-lutidineFL/FR
5-methyl quinoxalineFL/FR
2-methyl thio-3,5 or 6-methyl pyrazineFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
2,3,5-trimethyl pyrazineFL/FR
popcorn
2-acetyl pyrazineFL/FR
sulfurous
 benzothiazoleFL/FR
 furfuryl thioacetateFL/FR
2-methyl 5-(methyl thio) furanFL/FR
O-methyl S-1-methoxyhexan-3-yl carbonothioateFL/FR
vegetable
1-furfuryl pyrroleFL/FR
 tetrahydrofurfuryl alcoholFL/FR
woody
 juniper berry oleoresinFL/FR
 
For Flavor
 
No flavor group found for these
2,5-dimethyl-3-thiofuroyl furanFL
2-ethyl-3,5(or 6)-dimethyl pyrazineFL/FR
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
absinthe
 absinthe flavorFL
alliaceous
 benzyl mercaptanFL
 dicyclohexyl disulfideFL
 tropical thiazoleFL/FR
bitter
2-hydroxymethyl-6-methyl-pyridine 
brown
 fenugreek oleoresinFL/FR
1-hydroxy-2-butanoneFL/FR
burnt
 furfuryl alcoholFL
1-(2-furfuryl thio) propanoneFL
2-methyl quinoxalineFL
isopropenyl pyrazineFL/FR
2-(thienyl-2)-ethanethiol 
2,6-xylenolFL/FR
caramellic
 caramel furanoneFL
 cycloteneFL/FR
 fenugreek absoluteFL/FR
 fenugreek distillatesFL
chocolate
 mocha cream flavorFL
cocoa
 cocoa hexenalFL/FR
2-methyl furanFL
coffee
 cappuccino flavorFL
 chicory flavorFL
 chicory root 
 chicory root distillatesFL
 chicory root essenceFL
roasted chicory root oilFL
 chicory tinctureFL
 cichorium intybus root extractFL/FR
 cichorium intybus root solid extractFL/FR
roasted coffea arabica seed extractFL/FR
 coffea arabica seed extractFL/FR
 coffea arabica seed oilFL/FR
 coffea canephora seed extractFL
 coffee absoluteFL/FR
arabica coffee bean butterFL/FR
roasted coffee bean concentrateFL
roasted robusta coffee bean essenceFL
roasted arabica coffee bean essenceFL/FR
roasted coffee bean essenceFL
roasted coffee bean extractFL/FR
dried roasted coffee bean extractFL
roasted robusta coffee bean extractFL
roasted arabica coffee bean oil CO2 extractFL/FR
 coffee bean oil extractFL/FR
 coffee creme brulee flavorFL
 coffee difuranFL/FR
 coffee dioneFL/FR
 coffee distillatesFL
espresso coffee distillatesFL
 coffee enhancersFL
espresso coffee essenceFL
espresso coffee extractFL
dark roast coffee flavorFL
 coffee flavorFL
espresso coffee flavorFL
irish coffee flavorFL
 coffee liqueur flavorFL
 coffee pyrazineFL
 coffee resinoidFL/FR
 coffee royale flavorFL
 difurfuryl etherFL
 diisoamyl thiomalateFL
3,6-dimethyl pyrazine-2-thiol 
2,4-dimethyl thiazoleFL
2,5-dimethyl-3-furfurylthio-pyrazine 
2,5-dimethyl-3,6-diethyl pyrazine 
2-ethyl-4-methyl thiazoleFL/FR
 furfuryl mercaptanFL/FR
 methyl furfuryl disulfideFL/FR
 methyl furfuryl mercaptopropionateFL
2-methyl-5-vinyl pyrazineFL
2-isopropyl pyrazineFL
2-thiophene thiolFL
dairy
 creme brulle coffee flavorFL
earthy
 difurfuryl sulfideFL
fruity
 furfuryl propionateFL
fusel
2-methyl butyraldehydeFL/FR
green
3,4-dimethoxystyreneFL
2,6-dimethyl-gamma-thiopyrone 
2-methyl-5-isopropyl pyrazineFL
2-(1-propenyl) pyridine 
hazelnut
4-hydroxymethyl-pyridine 
malty
 malt flavorFL
meaty
 benzothiazoleFL/FR
3-mercapto-2-butanoneFL
2-methyl 3-(methyl thio) furanFL
mustard
 furfuryl methyl etherFL
musty
2-ethoxythiazoleFL
 menthofuranFL/FR
2-methyl 5-(methyl thio) furanFL/FR
 thymyl methyl etherFL/FR
2,3,5-trimethyl pyrazineFL/FR
nutty
2-acetyl furanFL/FR
3,5(6)-cocoa pyrazineFL
3,5-cocoa pyrazineFL/FR
2,6-dimethyl pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
4,5-dimethyl-2-ethyl-3-thiazolineFL/FR
 filbert heptenoneFL/FR
 hazelnut flavorFL
 hazelnut pasteFL
2,6-lutidineFL/FR
5-methyl quinoxalineFL/FR
2-methyl thio-3,5 or 6-methyl pyrazineFL/FR
2-methyl-3-pentyl pyrazine 
 nutty pyrazineFL/FR
 nutty thiazoleFL
 tetrahydrofurfuryl alcoholFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
onion
 furfuryl isopropyl sulfideFL
phenolic
2-pentenyl furan 
roasted
2-acetyl pyrazineFL/FR
roasted arabica coffee bean oilFL/FR
2,6-dimethyl-thio-gamma-pyrone 
 ethyl 3-(furfuryl thio) propionateFL
 furfuryl thioacetateFL/FR
O-methyl S-1-methoxyhexan-3-yl carbonothioateFL/FR
smoky
dextro-xyloseFL
spicy
 cinnamon hazelnut cappuccino flavorFL
sulfurous
 butyl mercaptanFL
 ethyl methyl sulfideFL
S-ethyl thioacetateFL
 furfuryl thiopropionateFL
3-methyl-2-butane thiolFL
2-thienyl mercaptanFL
vegetable
1-furfuryl pyrroleFL/FR
woody
 juniper berry oleoresinFL/FR
 
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Potential Uses:
 coffeeFL
 meatFL
 nutFL
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
2-furan methane thiol formate
S-(furan-2-ylmethyl) methanethioate
2-furanmethanethiol formate
2-2-furanmethanethiol formate
2-furanmethanethiolformate
3-(2-furanyl methyl) methane thioate
S-(2-furanyl methyl) methane thioate
3-(2-furanylmethyl) methanethioate
 furfuryl thioformate
 furfuryl thioformate (2-furanmethanethiol formate)
 furfuryl thiol formate
 furfurylthioformate
 furfurylthiol butyrate
 furfurylthiol formate
2-furyl methyl sulfanyl formaldehyde
 methane thioic acid 3-(2-furanyl methyl) ester
 methane thioic acid S-(2-furanyl methyl) ester
 methanethioic acid, 3-(2-furanylmethyl) ester
 methanethioic acid, S-(2-furanylmethyl) ester
Synonyms   Articles   Notes   Search   Top
Synonyms   Articles   Notes   Search   Top
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