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2-(2-chloroethyl)-2H-tetrazol-5-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15284-32-9

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15284-32-9 Usage

Chemical class

Tetrazole compounds

Usage

Synthetic intermediate in pharmaceutical industry

Molecular weight

160.59 g/mol

Physical form

White to off-white powder

Melting point

169-172°C

Primary use

Building block for preparation of novel heterocyclic compounds with potential biological activities

Reactivity

Versatile

Stability

High, making it valuable for medicinal and pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 15284-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15284-32:
(7*1)+(6*5)+(5*2)+(4*8)+(3*4)+(2*3)+(1*2)=99
99 % 10 = 9
So 15284-32-9 is a valid CAS Registry Number.

15284-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chloroethyl)tetrazol-5-amine

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:15284-32-9 SDS

15284-32-9Downstream Products

15284-32-9Relevant academic research and scientific papers

Evolving the Scope of 5,5’-Azobistetrazoles in the Search for High Performing Green Energetic Materials

Benz, Maximilian,Gruhne, Michael S.,Klap?tke, Thomas M.,Krüger, Nina,Lenz, Tobias,Lommel, Marcus,Stierstorfer, J?rg

, p. 4388 - 4392 (2021)

The azotetrazole moiety represents a great platform for energetic materials, it offers a planar and nitrogen-rich backbone, combined with a high heat of formation, which easily can be functionalized and tuned. Herein, we start from sodium 5-aminotetrazolate and obtain two isomers by substitution reaction with 2-chloroethanol. Azidoethyl and nitratoethyl substituted azo- tetrazoles were finally synthesized by oxidative azo coupling of the respective N-ethyl functionalized 5-aminotetrazole precursors using tert-butyl hypochlorite as reagent. All compounds were analyzed through multicore NMR and IR spectroscopy as well as mass spectrometry. All solid compounds were further investigated using low-temperature X-ray crystallography. The purity was verified by CHNO elemental analysis and the decomposition temperature (DTA) and sensitivities toward impact, friction and electrostatic discharged were determined. Based on the CBS-4M calculation results, the energetic properties were calculated using the EXPLO5 code.

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