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1754-62-7

1754-62-7 | Methyl trans-cinnamate

CAS No: 1754-62-7 Catalog No: AG003598 MDL No:MFCD00008458

Product Description

Catalog Number:
AG003598
Chemical Name:
Methyl trans-cinnamate
CAS Number:
1754-62-7
Molecular Formula:
C10H10O2
Molecular Weight:
162.1852
MDL Number:
MFCD00008458
IUPAC Name:
methyl (E)-3-phenylprop-2-enoate
InChI:
InChI=1S/C10H10O2/c1-12-10(11)8-7-9-5-3-2-4-6-9/h2-8H,1H3/b8-7+
InChI Key:
CCRCUPLGCSFEDV-BQYQJAHWSA-N
SMILES:
COC(=O)/C=C/c1ccccc1
EC Number:
203-093-8
UNII:
533CV2ZCQL
NSC Number:
9411
FEMA Number:
2698

Properties

Complexity:
167  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1  
Exact Mass:
162.068g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
162.188g/mol
Monoisotopic Mass:
162.068g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.6  

Literature

Title Journal
Insights into myalgic encephalomyelitis/chronic fatigue syndrome phenotypes through comprehensive metabolomics. Scientific reports 20180101
Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles. Nature chemical biology 20120501
Safety assessment of Zanthoxylum alatum Roxb. essential oil, its antifungal, antiaflatoxin, antioxidant activity and efficacy as antimicrobial in preservation of Piper nigrum L. fruits. International journal of food microbiology 20120201
Methyl cinnamate inhibits adipocyte differentiation via activation of the CaMKK2-AMPK pathway in 3T3-L1 preadipocytes. Journal of agricultural and food chemistry 20120201
BF3·OEt2-promoted diastereoselective diacetoxylation of alkenes by PhI(OAc)2. The Journal of organic chemistry 20111216
Chemical characterization and antimicrobial activity of rhizome essential oils of very closely allied Zingiberaceae species endemic to Borneo: Alpinia ligulata K. Schum. and Alpinia nieuwenhuizii Val. Chemistry & biodiversity 20110501
Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage. Bioorganic & medicinal chemistry 20110401
Ocotea quixos Lam. essential oil: in vitro and in vivo investigation on its anti-inflammatory properties. Fitoterapia 20100601
Inhibitory effects of methyl trans-cinnamate on mushroom tyrosinase and its antimicrobial activities. Journal of agricultural and food chemistry 20090325
Tricholoma matsutake 1-Ocen-3-ol and methyl cinnamate repel mycophagous Proisotoma minuta (Collembola: Insecta). Mycorrhiza 20080201
Yield and oil composition of 38 basil (Ocimum basilicum L.) accessions grown in Mississippi. Journal of agricultural and food chemistry 20080109
Antiplatelet and antithrombotic activities of essential oil from wild Ocotea quixos (Lam.) Kosterm. (Lauraceae) calices from Amazonian Ecuador. Pharmacological research 20070101
Fragrance material review on methyl cinnamate. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20070101
Esters, amides and substituted derivatives of cinnamic acid: synthesis, antimicrobial activity and QSAR investigations. European journal of medicinal chemistry 20041001
Determination of 2H/1H and 13C/12C isotope ratios of (E)-methyl cinnamate from different sources using isotope ratio mass spectrometry. Journal of agricultural and food chemistry 20040519
Inhibition of human immunodeficiency virus type-1 integrase by curcumin. Biochemical pharmacology 19950418

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