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methyl 3,4,5-trimethoxycinnamate
2-propenoic acid, 3-(3,4,5-trimethoxyphenyl)-, methyl ester, (2E)-

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CAS Number: 7560-49-8Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J103.536C
MDL:MFCD03614740
XlogP3-AA:2.10 (est)
Molecular Weight:252.26652000
Formula:C13 H16 O5
BioActivity Summary:listing
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
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Google Patents:Search
US Patents:Search
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Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 370.60 °C. @ 760.00 mm Hg (est)
Flash Point: 326.00 °F. TCC ( 163.50 °C. ) (est)
logP (o/w): 1.770 (est)
Soluble in:
 water, 583.5 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Methyl 3,4,5-trimethoxycinnamate >95%
Odor: characteristic
Use: Methyl 3,4,5-trimethoxycinnamate is a natural phenylpropanoid found in the herbs of Alstonia yunnanensis. Methyl 3,4,5-trimethoxycinnamate may have the production to protect the heart from arrhythmias via its inhibitory effect on calcium channel.
Matrix Scientific
For experimental / research use only.
Methyl 3,4,5-trimethoxycinnamate, 98%
 
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
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for methyl 3,4,5-trimethoxycinnamate usage levels up to:
 not for fragrance use.
 
Recommendation for methyl 3,4,5-trimethoxycinnamate flavor usage levels up to:
 not for flavor use.
 
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 :735846
National Institute of Allergy and Infectious Diseases:Data
methyl (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate
Chemidplus:0007560498
 
References:
 methyl (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):735846
Pubchem (sid):135102485
 
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
CHEBI:View
CHEMBL:View
Metabolomics Database:Search
HMDB (The Human Metabolome Database):HMDB38551
FooDB:FDB017938
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 pepper long pepper root
Search Trop Picture
 rauwolfia serpentina
Search Trop Picture
 
Synonyms:
 cinnamic acid, 3,4,5-trimethoxy-, methyl ester
 methyl (2E)-3-(3,4,5-trimethoxyphenyl)acrylate
 methyl (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate
 methyl 3,4,5-trimethyoxycinnamate
2-propenoic acid, 3-(3,4,5-trimethoxyphenyl)-, methyl ester, (2E)-
3,4,5-trimethoxycinnamic acid methyl ester
 

Articles:

PubMed:Potential antiarrhythmic effect of methyl 3,4,5-trimethoxycinnamate, a bioactive substance from roots of polygalae radix: suppression of triggered activities in rabbit myocytes.
PubMed:Chemical constituents of the whole plant of Elsholtzia rugulosa.
PubMed:New cytotoxic cyclobutanoid amides, a new furanoid lignan and anti-platelet aggregation constituents from Piper arborescens.
PubMed:Depigmenting activity and low cytotoxicity of alkoxy benzoates or alkoxy cinnamte in cultured melanocytes.
PubMed:A new gas chromatographic method for the estimation of reserpine and rescinnamine.
 
Notes:
Isol. from Piper longum (long pepper) and other plant spp.
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