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(2E)-3-(3,4-dimethoxyphenyl)-2-methylprop-2-enoic acid is a chemical compound with the molecular formula C12H14O4. It is a derivative of cinnamic acid and is commonly found in various plants. (2E)-3-(3,4-dimethoxyphenyl)-2-methylprop-2-enoic acid has a unique chemical structure and has been studied for its potential antioxidant and anti-inflammatory properties.

70570-20-6

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70570-20-6 Usage

Uses

Used in Pharmaceutical Industry:
(2E)-3-(3,4-dimethoxyphenyl)-2-methylprop-2-enoic acid is used as a potential therapeutic agent for various health conditions due to its potential antioxidant and anti-inflammatory properties. It has been investigated for its potential role in the development of new drugs and treatments.
Used in Cosmetic Industry:
(2E)-3-(3,4-dimethoxyphenyl)-2-methylprop-2-enoic acid is used as a skincare ingredient for its potential benefits in skincare products. It has been studied for its potential therapeutic and skincare benefits, making it a promising candidate for use in cosmetic formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 70570-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70570-20:
(7*7)+(6*0)+(5*5)+(4*7)+(3*0)+(2*2)+(1*0)=106
106 % 10 = 6
So 70570-20-6 is a valid CAS Registry Number.

70570-20-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(3,4-dimethoxyphenyl)-2-methylprop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 2-Methyl-3t-(3.4-dimethoxy-phenyl)-acrylsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:70570-20-6 SDS

70570-20-6Downstream Products

70570-20-6Relevant academic research and scientific papers

Very short and efficient syntheses of the spermine alkaloid kukoamine A and analogs using isolable succinimidyl cinnamates

Garnelis, Thomas,Athanassopoulos, Constantinos M.,Papaioannou, Dionissios,Eggleston, Ian M.,Fairlamb, Alan H.

, p. 264 - 265 (2007/10/03)

Direct selective acylation of the primary amino functions of spermine and spermidine with a variety of isolable succinimidyl cinnamates, followed by catalytic hydrogenation, gave high yields of the spermine alkaloid kukoamine A and analogs suitable for structure-activity relationship studies. Suitable succinimidyl cinnamates were readily obtained through Wittig reaction of aromatic aldehydes with the ylides Ph3P=CRCO2Me, followed by saponification and activation with N-hydroxysuccinimide in the presence of N,N'-dicyclohexylcarbodiimide. Copyright

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