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3-Hydroxy-4-methoxycinnamic acid, predominantly trans

ALDRICH/103012 - 97%

CAS Number: 537-73-5
Empirical Formula (Hill Notation): C10H10O4
Molecular Weight: 194.18
EC Number: 208-676-0
MDL Number: MFCD00004391
Linear Formula: HOC6H3(OCH3)CH=CHCO2H
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-103012-1G 1 g
 $0.00
1/EA
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45-103012-5G 5 g
 $204.00
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 103012-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 103012-5G

 

assay 97%
form solid
functional group carboxylic acid
InChI 1S/C10H10O4/c1-14-9-4-2-7(6-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)/b5-3+
InChI key QURCVMIEKCOAJU-HWKANZROSA-N
mp 230 °C (dec.) (lit.)
SMILES string COc1ccc(C=CC(O)=O)cc1O
Application: 3-Hydroxy-4-methoxycinnamic acid was used in the synthesis of tranilast and various tranilast analogs (cinnamoyl anthranilates) by genetically engineered Saccharomyces cerevisiae yeast strain. It was also used in the synthesis of glycoside compounds by undergoing glycosidation.
General description: 3-Hydroxy-4-methoxycinnamic acid, predominantly trans is available as white crystals. 3-Hydroxy-4-methoxycinnamic acid is isolated from the aerial part of Artemisia capillaris, Chinese medicinal plant. It is a component of chinese herbal medicine used for a pain killer and stomachic. It is an efficient acetylcholine inhibitor. 3-Hydroxy-4-methoxycinnamic acid is bioactive metabolite of Spilanthes acmella Murr. It increases the resistance of low-density lipoprotein (LDL) to oxidation.
Packaging: 1, 5 g in glass bottle
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
RIDADR NONH for all modes of transport
WGK Germany WGK 2
Purity 97%
mp 230 °C (dec.) (lit.)
UNSPSC 12352100

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