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2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, 2-methylpropyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59831-95-7

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59831-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59831-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,3 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59831-95:
(7*5)+(6*9)+(5*8)+(4*3)+(3*1)+(2*9)+(1*5)=167
167 % 10 = 7
So 59831-95-7 is a valid CAS Registry Number.

59831-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpropyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,3-(4-hydroxy-3-methoxyphenyl)-,2-methylpropyl ester

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:59831-95-7 SDS

59831-95-7Downstream Products

59831-95-7Relevant academic research and scientific papers

Biological activity evaluation and structure-activity relationships analysis of ferulic acid and caffeic acid derivatives for anticancer

Li, Weixia,Li, Nianguang,Tang, Yuping,Li, Baoquan,Liu, Li,Zhang, Xu,Fu, Haian,Duan, Jin-Ao

, p. 6085 - 6088 (2012/10/29)

The anticancer activities of alkyl esters and NO-donors of ferulic acid (FA) and caffeic acid (CA) were assessed by a high-throughout screening (HTS) method, and the structure-activity relationships were described. CA alkyl esters had better anticancer activities than FA alkyl esters with the same alkyl substituent. Mono-nitrates and phenylfuroxan nitrates were more potent than the dual nitrates. Phenylsulfonylfuroxan nitrates of FA, especially compounds 8b-8d, exhibited more potent activities in anticancer.

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