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41234-20-2

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41234-20-2 Usage

General Description

3-(2-bromo-4,5-dimethoxyphenyl)-2-cyanopropionic acid is a chemical compound with the chemical formula C12H13BrNO4. It is a cyanopropionic acid derivative that contains a bromo and two methoxy groups on a phenyl ring. 3-(2-bromo-4,5-dimethoxyphenyl)-2-cyanopropionic acid is used in organic synthesis and pharmaceutical research as a starting material or intermediate molecule. Its specific properties and potential applications are dependent on the substituent groups and functional groups present, making it a versatile compound with potential uses in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 41234-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,3 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41234-20:
(7*4)+(6*1)+(5*2)+(4*3)+(3*4)+(2*2)+(1*0)=72
72 % 10 = 2
So 41234-20-2 is a valid CAS Registry Number.

41234-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-bromo-4,5-dimethoxyphenyl)-2-cyanopropionic acid

1.2 Other means of identification

Product number -
Other names β-(2-Brom-4,5-dimethoxyphenyl)-α-cyanopropionsaeure

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:41234-20-2 SDS

41234-20-2Relevant articles and documents

A practical synthesis of 1-cyano-4,5-dimethoxybenzocyclobutene

Zhao, Sheng Yin,Liang, Hong Yu,Shao, Zhi Yu,Chen, Rui

, p. 420 - 422 (2009)

A practical synthesis of 1-cyano-4,5-dimethoxybenzocyclobutene, the key intermediate of Ivabradine, was developed in four or five steps using two different routes. 2-Bromo-4,5-dimethoxyhydrocinnamonitrile was produced via the condensation of 2-bromo-4,5-dimethoxybenzaldehyde with acetonitrile or cyanoacetic acid and reduction by NaBH4. Cyclisation gave 1-cyano-4,5-dimethoxybenzocyclobutene. Overall yields of the routes A and B were 30% and 37% respectively. Route B is a short and simple route, permitting the synthesis of 1-cyano-4,5-dimethoxybenzocyclobutene on a large scale.

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