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31995-60-5

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31995-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31995-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,9 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31995-60:
(7*3)+(6*1)+(5*9)+(4*9)+(3*5)+(2*6)+(1*0)=135
135 % 10 = 5
So 31995-60-5 is a valid CAS Registry Number.

31995-60-5SDS

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 5-Methyl-4-nitro-1H-1,2,3-benzotriazole

1.2 Other means of identification

Product number -
Other names 5-methyl-4-nitrobenzotriazole

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:31995-60-5 SDS

31995-60-5Relevant articles and documents

Synthesis of 6(5)-Methyl-5,7(4,6)-dinitro-1H-benzo[1.2.3]triazole under thermal conditions and under microwave irradiation

De Vekki

, p. 135 - 137 (2007)

6(5)-Methyl-5,7(4,6)-dinitro-1H-benzo[1.2.3]triazole was synthesized by nitration of 6(5)-methyl-7(4)-nitro-1H-benzo[1.2.3]triazole under thermal conditions and under microwave irradiation. Advantages of the microwave irradiation mode are shown.

Novel Dimroth Rearrangements of the Benzotriazole System: 4-Amino-1-(arylsulfonyl)benzotriazoles to 4-benzotriazoles

Katritzky, Alan R.,Ji, Fu-Bao,Fan, Wei-Qiang,Gallos, John K.,Greenhill, John V.,et al.

, p. 190 - 195 (2007/10/02)

A variety of mono- and diarylsulfonyl-substituted 4-aminobenzotriazoles were prepared.Thermal rearrangements of 4-amino-1-(arylsulfonyl)benzotriazoles to 4-benzotriazoles were observed and confirmed by separation of the rearrangement products.Their structures were characterized by spectral methods and by X-ray crystallography.The rearrangement rates were studied by variable-temperature NMR experiments.Crossover experiments support an intramolecular mechanism involving a heterolytic benzotriazole ring cleavage to form a diazo intermediate followed by recyclization to the 4-amino group.

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