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78827-54-0

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78827-54-0 Usage

Class of compound

Aziridine

Aziridine structure

Three-membered ring with a nitrogen atom

Butenyl group

Four-carbon chain with a double bond and a methyl group attached to the third carbon

Uses

a. Organic synthesis reactions
b. Preparation of complex organic molecules
c. Precursor in the production of pharmaceuticals and agrochemicals
d. Development of new materials
e. Chemical research

Safety

Handle with care and in accordance with proper safety protocols due to its chemical structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 78827-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,2 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78827-54:
(7*7)+(6*8)+(5*8)+(4*2)+(3*7)+(2*5)+(1*4)=180
180 % 10 = 0
So 78827-54-0 is a valid CAS Registry Number.

78827-54-0SDS

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 1-[(E)-3,3-dimethylbut-1-enyl]aziridine

1.2 Other means of identification

Product number -
Other names -

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:78827-54-0 SDS

78827-54-0Downstream Products

78827-54-0Relevant articles and documents

THE REACTION OF VINYL AZIDES WITH SULFOXONIUM YLIDS. SYNTHESIS OF N-VINYL TRIAZOLINES AND VINYL AZIRIDINES.

Hassner, Alfred,Belinka, Benjamin A.,Haber, Mark,Munger, Paul

, p. 1863 - 1866 (2007/10/02)

Vinyl azides 1 react with dimethylsulfoxonium ylid 3 at the azide function to produce in high yield 1-vinyl-4,5-unsubstituted-Δ2-1,2,3-triazolines 4.Vacuum flash pyrolysis of 4 furnished N-vinylaziridines 7 without formation of pyrrolines.

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