100032-79-9 Usage
Description
4-BROMO-2-NITROPHENYLHYDRAZINE HYDROCHLORIDE is a chemical compound that serves as a reagent in the synthesis of pharmaceuticals and organic compounds. It is a hydrazine derivative featuring a nitro group and a bromo substituent on a phenyl ring, known for its versatility in reacting with various functional groups in organic molecules.
Used in Pharmaceutical Industry:
4-BROMO-2-NITROPHENYLHYDRAZINE HYDROCHLORIDE is used as an intermediate for the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds due to its ability to react with different functional groups.
Used in Dye Industry:
In the dye industry, 4-BROMO-2-NITROPHENYLHYDRAZINE HYDROCHLORIDE is used as an intermediate for the production of dyes, leveraging its chemical properties to create a range of colorants for various applications.
Used in Pesticide Industry:
4-BROMO-2-NITROPHENYLHYDRAZINE HYDROCHLORIDE is used as a component in the synthesis of pesticides, playing a role in developing effective agents for agricultural and environmental purposes.
It is important to handle 4-BROMO-2-NITROPHENYLHYDRAZINE HYDROCHLORIDE with care, as it is toxic and potentially hazardous if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 100032-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100032-79:
(8*1)+(7*0)+(6*0)+(5*0)+(4*3)+(3*2)+(2*7)+(1*9)=49
49 % 10 = 9
So 100032-79-9 is a valid CAS Registry Number.
100032-79-9Relevant articles and documents
Design, synthesis and biological evaluation of 7-nitro-1H-indole-2- carboxylic acid derivatives as allosteric inhibitors of fructose-1,6- bisphosphatase
Bie, Jianbo,Liu, Shuainan,Zhou, Jie,Xu, Bailing,Shen, Zhufang
, p. 1850 - 1862 (2014/03/21)
A series of novel indole derivatives was synthesized as inhibitors of fructose-1,6-bisphosphatase (FBPase). Extensive structure-activity relationships were conducted and led to a potent FBPase inhibitor 3.9 with an IC50 of 0.99 μM. The binding mode of this series of indoles was predicted using CDOCKER algorithm. The results of this research will shed light on the further design and optimization of novel small molecules as FBPase inhibitors.
