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31163-65-2

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31163-65-2 Usage

Physical form

Yellow crystalline solid

Uses

Production of pharmaceuticals, dyes, and other organic compounds

Classification

High-energy material

Potential applications

Explosive or propellant, chemical warfare agents

Reactivity

Highly reactive and unstable

Handling precautions

Must be handled with caution in controlled laboratory settings due to instability.

Check Digit Verification of cas no

The CAS Registry Mumber 31163-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31163-65:
(7*3)+(6*1)+(5*1)+(4*6)+(3*3)+(2*6)+(1*5)=82
82 % 10 = 2
So 31163-65-2 is a valid CAS Registry Number.

31163-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dinitroindazole

1.2 Other means of identification

Product number -
Other names 2,7=Dinitroindazol

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:31163-65-2 SDS

31163-65-2Upstream product

31163-65-2Downstream Products

31163-65-2Relevant articles and documents

Azoles. Part 32: Nitroindazole derivatives and their electron affinity

Usarewicz,Wrzeciono,Lukaszewski,Gatniejewska,Peisert

, p. 15 - 18 (2007/10/02)

A modified procedure for the synthesis of the dinitroindazoles 5-8 is described. Treatment of the chloronitro- and dinitroindazoles 1-8 with epichlorohydrin afforded the chlorohydroxypropyl- and epoxypropylindazole derivatives 2a-8a, 1b-5b, 7b and 7c. The structure of the compounds is confirmed by the aid of their IR, 1H and 13C NMR spectra. The electron affinity of the nitroindazole derivatives 1-16 is discussed on the basis of their halfwave potentials and in the combination with their eventual radiosensitizing properties.

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