epimyrtine
 
Notes:
None found
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CAS Number: 82111-02-2Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web: J640.754D
XlogP3-AA: 1.10 (est)
Molecular Weight: 167.25169000
Formula: C10 H17 N O
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
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Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
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
Soluble in:
 water, 8.109e+004 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:
None found
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Suppliers:
 None found
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Safety Information:
 
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
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for epimyrtine usage levels up to:
 not for fragrance use.
 
Recommendation for epimyrtine 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 ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 10866719
National Institute of Allergy and Infectious Diseases: Data
 (4R,9aS)-4-methyl-1,3,4,6,7,8,9,9a-octahydroquinolizin-2-one
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References:
 (4R,9aS)-4-methyl-1,3,4,6,7,8,9,9a-octahydroquinolizin-2-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 10866719
Pubchem (cas): 82111-02-2
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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
HMDB (The Human Metabolome Database): HMDB30371
FooDB: FDB002219
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: 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
 Vaccinium myrtillus shoot
Search Trop  Picture
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Synonyms:
(4R,9aS)-4-methyl-1,3,4,6,7,8,9,9a-octahydroquinolizin-2-one
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Articles:
PubMed: Modifications in nitric oxide and superoxide anion metabolism induced by fructose overload in rat heart are prevented by (-)-epicatechin.
PubMed: Total synthesis of (-)-epimyrtine by a gold-catalyzed hydroamination approach.
PubMed: Stereoselective synthesis of 2,6-cis- and 2,6-trans-piperidines through organocatalytic aza-Michael reactions: a facile synthesis of (+)-myrtine and (-)-epimyrtine.
PubMed: Synthetic applications of sulfur-substituted indolizidines and quinolizidines.
PubMed: Recent Applications of Imines as Key Intermediates in the Synthesis of Alkaloids and Novel Nitrogen Heterocycles.
PubMed: Iminium Ion Cascade Reactions: Stereoselective Synthesis of Quinolizidines and Indolizidines.
PubMed: A convenient allylsilane-N-acyliminium route toward indolizidine and quinolizidine alkaloids.
PubMed: Indolizidine and quinolizidine alkaloids.
PubMed: Cascade iminium ion reactions for the facile synthesis of quinolizidines. Concise syntheses of (+/-)-epilupinine and (-)-epimyrtine.
PubMed: Asymmetric synthesis of the quinolizidine alkaloid (-)-epimyrtine with intramolecular Mannich cyclization and N-sulfinyl delta-amino beta-ketoesters.
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