Home Other Building Blocks 2-methoxy-3-phenylprop-2-enoic acid

2-methoxy-3-phenylprop-2-enoic acid

CAS No.:
1081778-14-4
Catalog Number:
AG01BE28
Molecular Formula:
C10H10O3
Molecular Weight:
178.1846
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Product Description
Catalog Number:
AG01BE28
Chemical Name:
2-methoxy-3-phenylprop-2-enoic acid
CAS Number:
1081778-14-4
Molecular Formula:
C10H10O3
Molecular Weight:
178.1846
MDL Number:
MFCD00799235
IUPAC Name:
2-methoxy-3-phenylprop-2-enoic acid
InChI:
InChI=1S/C10H10O3/c1-13-9(10(11)12)7-8-5-3-2-4-6-8/h2-7H,1H3,(H,11,12)
InChI Key:
CNXZMGRWEYQCOQ-UHFFFAOYSA-N
SMILES:
COC(=Cc1ccccc1)C(=O)O
Properties
Complexity:
202  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
178.063g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
178.187g/mol
Monoisotopic Mass:
178.063g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
46.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
1  
XLogP3:
2.1  
Literature
Title Journal
Effects of pre- and postnatal exposure to the UV-filter octyl methoxycinnamate (OMC) on the reproductive, auditory and neurological development of rat offspring. Toxicology and applied pharmacology 20110201
Octyl methoxycinnamate modulates gene expression and prevents cyclobutane pyrimidine dimer formation but not oxidative DNA damage in UV-exposed human cell lines. Toxicological sciences : an official journal of the Society of Toxicology 20100401
Efficacy of octyl methoxycinnamate in preventing postoperative peritoneal adhesions: an experimental model. The journal of obstetrics and gynaecology research 20091201
An updated review of tyrosinase inhibitors. International journal of molecular sciences 20090601
Photostability of commercial sunscreens upon sun exposure and irradiation by ultraviolet lamps. BMC dermatology 20070101
Changes in ultraviolet absorbance and hence in protective efficacy against lipid peroxidation of organic sunscreens after UVA irradiation. Journal of photochemistry and photobiology. B, Biology 20060301
Method to overcome photoreaction, a serious drawback to the use of dichlorofluorescin in evaluation of reactive oxygen species. Biochemical and biophysical research communications 20030516
Photosensitive dermatitis due to sunscreen allergy in a child. The Australasian journal of dermatology 20020501
The effect of UV absorbing sunscreens on the reflectance and the consequent protection of skin. Photochemistry and photobiology 20020201
Report of 19 cases of photoallergic contact dermatitis to sunscreens seen at the Skin and Cancer Foundation. The Australasian journal of dermatology 20011101
Properties