72635-78-0 Usage
General Description
3-Amino-4-bromobenzonitrile is a synthetic chemical compound belonging to the category of organic compounds known as benzene and substituted derivatives. These are aromatic compounds that contain one monocyclic ring, which is benzene, and are substituted with different functional groups. In this molecule specifically, the benzene ring is substituted with an amino, bromine, and nitrile group at specific positions. It is most commonly used in research or chemical reactions due to its structural properties. As with all chemicals, handling and use of 3-Amino-4-bromobenzonitrile should be performed with appropriate protection, as it may have harmful effects, but comprehensive data on its safety or potential hazard effects is not readily available.
Check Digit Verification of cas no
The CAS Registry Mumber 72635-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,3 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72635-78:
(7*7)+(6*2)+(5*6)+(4*3)+(3*5)+(2*7)+(1*8)=140
140 % 10 = 0
So 72635-78-0 is a valid CAS Registry Number.
72635-78-0Relevant articles and documents
SUBSTITUTED 2-AZA-BICYCLO[2.2.1]HEPTANE-3-CARBOXYLIC ACID (BENZYL-CYANO-METHYL)-AMIDES INHIBITORS OF CATHEPSIN C
-
Page/Page column 250, (2014/09/29)
This invention relates to 2-Aza-bicyclo[2.2.1]heptane-3-carboxylic acid (benzyl-cyano-methyl)- amides of formula (1) and their use as inhibitors of Cathepsin C, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of diseases connected with dipeptidyl peptidase I activity, e.g. respiratory diseases.
Electrophilic bromination of meta-substituted anilines with N-bromosuccinimide: Regioselectivity and solvent effect
Bartoli, Sandra,Cipollone, Amalia,Squarcia, Antonella,Madami, Andrea,Fattori, Daniela
experimental part, p. 1305 - 1308 (2009/12/24)
N-Bromosuccinimide-mediated electrophilic aromatic bromination of a series of anilines substituted with an electron-with-drawing group in the meta position was investigated. The regioselectivity of the reaction is markedly dependent on the polarity of the solvent and the bromination reaction can be tuned by appropriate selection of the reaction medium. Georg Thieme Verlag Stuttgart.
