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70321-36-7

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70321-36-7 Usage

General Description

2-Bromoacrylamide is a chemical compound with the molecular formula C3H4BrNO. It is a white crystalline solid that is typically used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 2-Bromoacrylamide is a versatile building block for the preparation of a variety of functionalized compounds due to its reactivity towards various nucleophiles and electrophiles. It can also be used as a monomer in the production of polymers and copolymers. The compound is known to be toxic and may cause irritation upon contact with skin or eyes, and inhalation of its vapors. Therefore, proper safety precautions should be taken when handling 2-Bromoacrylamide.

Check Digit Verification of cas no

The CAS Registry Mumber 70321-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,2 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70321-36:
(7*7)+(6*0)+(5*3)+(4*2)+(3*1)+(2*3)+(1*6)=87
87 % 10 = 7
So 70321-36-7 is a valid CAS Registry Number.

70321-36-7SDS

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-bromoprop-2-enamide

1.2 Other means of identification

Product number -
Other names 2-bromoacrylic acid amide

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:70321-36-7 SDS

70321-36-7Upstream product

70321-36-7Relevant articles and documents

How Reaction Conditions May Influence the Regioselectivity in the Synthesis of 2,3-Dihydro-1,4-benzoxathiine Derivatives

Casiraghi, Andrea,Valoti, Ermanno,Suigo, Lorenzo,Artasensi, Angelica,Sorvillo, Erica,Straniero, Valentina

, p. 13217 - 13227 (2018/10/24)

The exploration of different reaction conditions aiming to obtain both 2,3-dihydro-1,4-benzoxathiine-2-yl derivatives and 2,3-dihydro-1,4-benzoxathiine-3-yl ones is reported. The treatment of 1,2-mercaptophenol with an organic base and a specific 2-bromo acrylate results in a solvent- and substrate-dependent exclusive solvation of O- and S-anions, thus managing the regioselectivity.

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