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2-Bromoprop-2-en-1-amine, also known as 2-bromoallylamine, is an organic compound with the chemical formula C3H6BrN. It is a colorless liquid with a pungent odor and is soluble in water. 2-bromoprop-2-en-1-amine is a halogenated derivative of allylamine, featuring a bromine atom attached to the terminal carbon of the allyl group. 2-Bromoprop-2-en-1-amine is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is important to handle 2-bromoprop-2-en-1-amine with care, as it can be toxic and may cause irritation to the skin, eyes, and respiratory system.

6943-51-7

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6943-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6943-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6943-51:
(6*6)+(5*9)+(4*4)+(3*3)+(2*5)+(1*1)=117
117 % 10 = 7
So 6943-51-7 is a valid CAS Registry Number.

6943-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoprop-2-en-1-amine

1.2 Other means of identification

Product number -
Other names ALLYLAMINE,2-BROMO

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:6943-51-7 SDS

6943-51-7Relevant academic research and scientific papers

One-Pot Copper-Catalyzed Three-Component Reaction of Sulfonyl Azides, Alkynes, and Allylamines to Access 2,3-Dihydro-1 H-imi-dazo[1,2-a]indoles

Jin, Hongwei,Liu, Daohong,Liu, Yunkui,Zhou, Bingwei

supporting information, p. 1417 - 1424 (2020/04/27)

A copper-catalyzed multicomponent reaction of sulfonyl azides, alkynes, and allylamines affording 2,3-dihydro-1 H-imidazo-[1,2-a]indoles in moderate yields is reported. Four C-N bonds are constructed- by way of azide-alkyne cycloaddition (CuAAC) and double Ullmann-type coupling reactions in a one-pot process.

Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Fort, Diego A.,Woltering, Thomas J.,Nettekoven, Matthias,Knust, Henner,Bach, Thorsten

supporting information, p. 2989 - 2991 (2013/05/09)

Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H)-furanones resulted in rigid products (53-75%) with three spatially defined positions for further functionalisation. The Royal Society of Chemistry.

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