89607-19-2 Usage
Pyrazole derivative
A compound based on the pyrazole ring, which is a five-membered heterocyclic ring with two nitrogen atoms.
Carboxylic acid group
A functional group (-COOH) attached to the pyrazole ring, contributing to the compound's acidic properties.
Two nitro substituents
Two nitro groups (-NO2) attached to the pyrazole ring, which may enhance the compound's reactivity and potential hazard.
Potential use as an explosive material
Due to the presence of nitro groups, the compound may possess explosive properties and be suitable for use in explosives.
Precursor in the synthesis of other organic compounds
The compound can be used as a starting material or intermediate in the synthesis of various other organic compounds.
Applications in organic chemistry and material science
The compound may have potential applications in these fields due to its unique structure and properties.
Potential hazard
The presence of nitro groups in the molecule suggests that it could be potentially hazardous, requiring proper safety precautions and careful handling.
Check Digit Verification of cas no
The CAS Registry Mumber 89607-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,0 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89607-19:
(7*8)+(6*9)+(5*6)+(4*0)+(3*7)+(2*1)+(1*9)=172
172 % 10 = 2
So 89607-19-2 is a valid CAS Registry Number.
89607-19-2Relevant academic research and scientific papers
Perevalov, V. P.,Andreeva, M. A.,Baryshnenkova, L. I.,Manaev, Yu. A.,Yamburg, G. S.,et al.
, p. 1326 - 1330 (1983)
3-Bromo-1,5-dimethyl-4-nitropyrazole does not react upon heating with aqueous ammonia, while 1,5-dimethyl-3,4-dinitropyrazole under the same conditions yields 3-amino-1,5-dimethyl-4-nitropyrazole, which is formed from 3-bromo-1,5-dimethyl-4-nitropyrazole in the presence of a copper catalyst.The amination of 1-methyl-3,4-dinitropyrazole-5-carboxylic acid is accompanied by decarboxylation, which is characteristic for 4-substituted 1-methylpyrazole-5-carboxylic acids upon heating in aqueous ammonia or water.
