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1-Propen-1-amine, N-1-propenyl-, also known as allylamine, is an organic compound with the chemical formula C3H7N. It is a colorless, flammable liquid with a pungent, fishy odor. This primary amine is a derivative of propene, where one hydrogen atom is replaced by an amino group (-NH2). Allylamine is used as a building block in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and polymers. It is also used as a cross-linking agent in the production of polyurethane foams and as a curing agent for epoxy resins. Due to its reactivity, allylamine can be hazardous and requires proper handling and storage.

78982-46-4

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78982-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78982-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,8 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78982-46:
(7*7)+(6*8)+(5*9)+(4*8)+(3*2)+(2*4)+(1*6)=194
194 % 10 = 4
So 78982-46-4 is a valid CAS Registry Number.

78982-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(propen-1-yl)amine

1.2 Other means of identification

Product number -
Other names dipropyl enamine

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:78982-46-4 SDS

78982-46-4Relevant academic research and scientific papers

Synthesis of 2-ethyl-3,5-dimethylpyridine by heterocyclization of allylamine, cyclopropylamine, and diallylamine in the presence of palladium complexes

Atnabaeva,Muslimov,Khusnutdinov,Dzhemilev

body text, p. 1831 - 1835 (2009/09/06)

2-Ethyl-3,5-dimethylpyridine was synthesized by disproportionation and heterocyclization of allylamine, cyclopropylamine, and diallylamine in the presence of palladium catalysts.

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