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1H-Indazole, 3,5,7-trinitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64030-97-3

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64030-97-3 Usage

Physical form

Pale yellow solid

Hazard class

Highly explosive and unstable

Common uses

Military munitions, fireworks, propellants, and pyrotechnics

Handling precautions

High sensitivity to impact, friction, and static electricity

Regulatory status

Use is highly regulated and controlled due to potential hazards

Safety measures

Strict safety protocols required to prevent accidents and ensure safe handling

Check Digit Verification of cas no

The CAS Registry Mumber 64030-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,3 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64030-97:
(7*6)+(6*4)+(5*0)+(4*3)+(3*0)+(2*9)+(1*7)=103
103 % 10 = 3
So 64030-97-3 is a valid CAS Registry Number.

64030-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5,7-trinitro-1H-indazole

1.2 Other means of identification

Product number -
Other names 1H-Indazole,3,5,7-trinitro

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:64030-97-3 SDS

64030-97-3Upstream product

64030-97-3Downstream Products

64030-97-3Relevant academic research and scientific papers

Formation of 3,3,5,7-tetranitrooxindole and 3,5,7-trinitroindazole by nitration of oxindole

Bergman, Jan,Bergman, Solveig

, p. 9263 - 9266 (2007/10/03)

Nitration (HNO3/H2SO4) of oxindole gave 3,3,5,7-tetranitrooxindole (1c), which readily underwent ring-opening and decarboxylation to 4,6-dinitro-2-(dinitromethyl)aniline (4b), which in turn could be cyclized to 3,5,7-trinitroindazole (5).

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