thioacetanilide
ethanethioamide, N-phenyl-
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      637-53-6 Thioacetanilide
       
  • TCI AMERICA
    • TCI AMERICA
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      Product(s):
      T0188 Thioacetanilide >98.0%(N)
       
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CAS Number: 637-53-6Picture of molecule3D/inchi
Other(deleted CASRN): 22768-70-3
ECHA EINECS - REACH Pre-Reg: 211-288-4
FDA UNII: L9AL2GO03Y
Nikkaji Web: J6.915I
Beilstein Number: 2205727
MDL: MFCD00004942
XlogP3: 1.70 (est)
Molecular Weight: 151.23173000
Formula: C8 H9 N S
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: antioxidants
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
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US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 76.00 °C. @ 760.00 mm Hg
Boiling Point: 225.10 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.014000 mmHg (est)
Flash Point: 194.00 °F. TCC ( 89.90 °C. ) (est)
logP (o/w): 1.710
Soluble in:
 water, 2596 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: antioxidants
bleaching agents
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Suppliers:
BOC Sciences
For experimental / research use only.
Thioacetanilide
Santa Cruz Biotechnology
For experimental / research use only.
Thioacetanilide
Sigma-Aldrich: Aldrich
For experimental / research use only.
Thioacetanilide 98%
TCI AMERICA
For experimental / research use only.
Thioacetanilide >98.0%(N)
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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:
oral-guinea pig LD50  1775 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: DYSPNEA BEHAVIORAL: ATAXIA
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(2), Pg. 72, 1986.

intraperitoneal-mouse LD50  300 mg/kg
National Technical Information Service. Vol. AD277-689

oral-mouse LD50  2625 mg/kg
LUNGS, THORAX, OR RESPIRATION: DYSPNEA BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: ATAXIA
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(2), Pg. 72, 1986.

oral-rat LD50  2635 mg/kg
BEHAVIORAL: ATAXIA BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(2), Pg. 72, 1986.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: antioxidants
Recommendation for thioacetanilide usage levels up to:
 not for fragrance use.
 
Recommendation for thioacetanilide flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 637-53-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 820777
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 N-phenylethanethioamide
Chemidplus: 0000637536
RTECS: AE7350000 for cas# 637-53-6
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References:
 N-phenylethanethioamide
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 820777
Pubchem (sid): 134978518
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2930.90.2900
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 ethanethioamide, N-phenyl-
N-phenyl thioacetamide
1-(phenylamino)ethane-1-thione
N-phenylethanethioamide
N-phenylethanthioamid
N-phenylthioacetamide
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Articles:
PubMed: Arylazolylthioacetanilide. Part 11: design, synthesis and biological evaluation of 1,2,4-triazole thioacetanilide derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors.
PubMed: Arylazolyl(azinyl)thioacetanilides. Part 10: design, synthesis and biological evaluation of novel substituted imidazopyridinylthioacetanilides as potent HIV-1 inhibitors.
PubMed: Arylazolyl(azinyl)thioacetanilide. Part 9: Synthesis and biological investigation of thiazolylthioacetamides derivatives as a novel class of potential antiviral agents.
PubMed: 1,2,3-thiadiazole thioacetanilides. Part 2: Synthesis and biological evaluation of a new series of 2-{[4-(3,4-dichlorophenyl)-1,2,3-thiadiazol-5-yl]sulfanyl}acetanilides as HIV-1 inhibitors.
PubMed: 1,2,3-Selenadiazole thioacetanilides: synthesis and anti-HIV activity evaluation.
PubMed: Synthesis and biological evaluation of imidazole thioacetanilides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors.
PubMed: Application of beta-(2-chloroaroyl)thioacetanilide in synthesis(III): an efficient three-component synthesis of thiochromeno[2,3-b]pyridines catalyzed by KF/neutral Al2O3 co-operated with PEG 6000 under microwave irradiation.
PubMed: 1,2,3-Thiadiazole thioacetanilides as a novel class of potent HIV-1 non-nucleoside reverse transcriptase inhibitors.
PubMed: Thioacetanilide at 120 K.
PubMed: Application of beta-(2-chloroaroyl) thioacetanilides in synthesis: an unusual and highly efficient access to thiochromeno[2,3-b]pyridine derivatives.
PubMed: Synthesis and biological evaluation of new 3-substituted indole derivatives as potential anti-inflammatory and analgesic agents.
PubMed: Tetrazole thioacetanilides: potent non-nucleoside inhibitors of WT HIV reverse transcriptase and its K103N mutant.
PubMed: Synthesis, anticonvulsant, and anti-inflammatory evaluation of some new benzotriazole and benzofuran-based heterocycles.
PubMed: Correlation analyses for bimolecular nucleophilic substitution reactions of chloroacetanilide herbicides and their structural analogs with environmentally relevant nucleophiles.
PubMed: Optical analysis of the cirrhotic liver by near-infrared time-resolved spectroscopy.
PubMed: [Substantiation of maximum permissible levels of thioacylanilide in the air of work areas].
PubMed: The metabolism of thioacetanilide in the rat.
PubMed: Determination of some organic thio-compounds by precipitation of mercuric sulphide from mercury(II) ammine complexes-I Determination of thioacetamide and thioacetanilide.
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