94832-15-2 Usage
Uses
Used in Pharmaceutical Industry:
O-[4-Nitro-2-(trifluoromethyl)phenyl]hydroxylamine is used as an intermediate for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
O-[4-Nitro-2-(trifluoromethyl)phenyl]hydroxylamine is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Inflammatory and Neurodegenerative Disease Treatment:
O-[4-Nitro-2-(trifluoromethyl)phenyl]hydroxylamine is a potent inhibitor of nitric oxide synthase, an enzyme responsible for the production of nitric oxide in the body. Its inhibitory effect makes it a potential candidate for the development of drugs for the treatment of inflammatory and neurodegenerative diseases, where nitric oxide plays a significant role in disease progression.
Check Digit Verification of cas no
The CAS Registry Mumber 94832-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,3 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94832-15:
(7*9)+(6*4)+(5*8)+(4*3)+(3*2)+(2*1)+(1*5)=152
152 % 10 = 2
So 94832-15-2 is a valid CAS Registry Number.
94832-15-2Relevant academic research and scientific papers
Indole-type derivatives as inhibitors of p38 kinase
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Page/Page column 78, (2008/06/13)
The invention is directed to methods to inhibit p38-α kinase using compounds comprising a phenyl or thienyl coupled through a piperidine or piperazine nucleus to an indole residue wherein the indole residue mandatorily has a substituent on the ring nitrogen which is an amino or substituted amino group.
IMPROVED REAGENTS FOR N-AMINATION
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Page 4-5, (2010/02/06)
Improved reagents and methods of amination are provided. The reagents are phenyl hydroxylamines containing one nitro and at least one CF3 substituent on the phenyl moiety.
