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Allyl azide, with the chemical formula C3H5N3, is a colorless, unstable, and highly reactive liquid. It is an organic compound that contains an azide functional group (N3) attached to an allyl group (C3H5). Allyl azide is synthesized through the reaction of allyl bromide with sodium azide in the presence of a phase-transfer catalyst. Due to its high reactivity, it is used as a chemical intermediate in the synthesis of various organic compounds, such as pharmaceuticals and agrochemicals. It is also employed in the preparation of azido-containing polymers and as a reagent in click chemistry. However, it is important to handle allyl azide with extreme caution, as it is sensitive to heat, shock, and friction, and can decompose explosively.

821-13-6

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821-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 821-13-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 821-13:
(5*8)+(4*2)+(3*1)+(2*1)+(1*3)=56
56 % 10 = 6
So 821-13-6 is a valid CAS Registry Number.

821-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-azidoprop-1-ene

1.2 Other means of identification

Product number -
Other names 3-Azido-propen

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:821-13-6 SDS

821-13-6Relevant academic research and scientific papers

Micellar promoted multi-component synthesis of 1,2,3-triazoles in water at room temperature

Tasca, Elena,La Sorella, Giorgio,Sperni, Laura,Strukul, Giorgio,Scarso, Alessandro

, p. 1414 - 1422 (2015/03/18)

Micellar media in water provide a simple and efficient environment favoring the multi-component synthesis of 1,2,3-triazoles from organic bromides, sodium azide and terminal alkynes in the presence of [Cu(IMes)Cl] 1 catalyst at room temperature within a f

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