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200956-55-4

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200956-55-4 Usage

General Description

Benzamide, 3-bromo-4-methoxy- is a chemical compound with the molecular formula C8H8BrNO2. It is a derivative of benzamide, which is an organic compound with the formula C6H5CONH2. The addition of a bromine atom and a methoxy group to the benzene ring in benzamide forms 3-bromo-4-methoxy-benzamide. benzamide, 3-bromo-4-methoxy- is commonly used as a building block in organic synthesis and medicinal chemistry. It has potential applications in the development of pharmaceuticals and agrochemicals due to its structural versatility and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 200956-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,9,5 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 200956-55:
(8*2)+(7*0)+(6*0)+(5*9)+(4*5)+(3*6)+(2*5)+(1*5)=114
114 % 10 = 4
So 200956-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrNO2/c1-12-7-3-2-5(8(10)11)4-6(7)9/h2-4H,1H3,(H2,10,11)

200956-55-4SDS

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 3-bromo-4-methoxybenzamide

1.2 Other means of identification

Product number -
Other names 3-Bromo-4-methoxy-benzamide

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:200956-55-4 SDS

200956-55-4Relevant articles and documents

1,3-Dibromo-5,5-dimethylhydantoin mediated oxidative amidation of terminal alkenes in water

Ma, Chunhua,Fan, Guojie,Wu, Ping,Li, Zhi,Zhou, Yang,Ding, Qingjie,Zhang, Wei

, p. 9889 - 9894 (2017)

A variety of terminal alkenes were converted to the corresponding amides in yields of 25 to 86% in water via treatment with 1,3-dibromo-5,5-dimethylhydantoin, followed by reaction with molecular iodine and aq. NH3 (or amine) in one pot. This metal- and organic solvent-free protocol is not only suitable for styrene derivatives, but also, for the first time, works well on terminal aliphatic alkenes.

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