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Bromamide, also known as 2-bromo-2-methylpropanamide, is an organic compound with the chemical formula C4H8BrNO. It is a derivative of acetamide, where one hydrogen atom is replaced by a bromine atom, and the methyl group is attached to the carbon adjacent to the amide group. Bromamide is a colorless, crystalline solid that is soluble in water and various organic solvents. It is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, bromamide can undergo various chemical transformations, such as nucleophilic substitution, making it a valuable building block in organic synthesis.

332-69-4

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332-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332-69-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 332-69:
(5*3)+(4*3)+(3*2)+(2*6)+(1*9)=54
54 % 10 = 4
So 332-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15BrN2O/c1-14(2)11(15)7-8-13-10-5-3-9(12)4-6-10/h3-6,13H,7-8H2,1-2H3

332-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Bromamide

1.2 Other means of identification

Product number -
Other names 3-[(4-bromophenyl)amino]-N,N-dimethyl-propanamide

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:332-69-4 SDS

332-69-4Downstream Products

332-69-4Relevant academic research and scientific papers

Method for catalyzing amino protection by imidazole hydrochloride

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Paragraph 0039-0043, (2019/08/01)

The invention provides an amino protection method which realizes multi-substituted amino protection by using imidazole hydrochloric acid as an accelerator to push derivatives of primary amine, secondary amine and acrylamide to perform Michael addition at a relatively low temperature, wherein the imidazole hydrochloric acid promotes a carbon-nitrogen bond to crack back to the derivatives of primaryamine and acrylamide at a high temperature. The method provided by the invention is simple and economical, high in practicability, free of any other catalysts or additives, capable of protecting amino to have good functional group tolerance and excellent yield and purity, short in reaction time, free from harsh reaction conditions and suitable for industrial production.

Michael addition reaction catalyzed by imidazolium chloride to protect amino groups and construct medium ring heterocycles

Dai, Zeshu,Li, Dan,Li, Yanwu,Li, Zhiyao,Luo, Wen,Shang, Suqin,Tian, Qingqiang,Wang, Xuetong,Yuan, Jianyong,Zhang, Ying

supporting information, (2019/12/04)

An effective approach for amino protection and construction of a seven-membered ring has been developed. The method uses imidazolium chloride to carry out the Michael addition reaction at low temperatures and perform amino deprotection or construction of a seven-membered ring at high temperatures.

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