108574-73-8 Usage
Molecular Structure
2-(4-chlorophenylamino)acetic acid isopropyl ester is an ester derivative of 2-(4-chlorophenylamino)acetic acid, with an isopropyl group attached to the acid component.
Chemical Properties
As an ester, it can undergo hydrolysis reactions to form the corresponding acid and alcohol. It can also participate in other organic reactions such as condensation and substitution.
Industrial Applications
It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as a building block in the production of organic compounds, and as an additive in the manufacture of plastics and polymers.
Research Uses
2-(4-chlorophenylamino)acetic acid isopropyl ester is often employed in the development of new chemical entities for medicinal purposes and in various research applications.
Versatility
Its use in the production of organic compounds, pharmaceuticals, agrochemicals, and plastics and polymers demonstrates its versatility and wide range of applications in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 108574-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,5,7 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108574-73:
(8*1)+(7*0)+(6*8)+(5*5)+(4*7)+(3*4)+(2*7)+(1*3)=138
138 % 10 = 8
So 108574-73-8 is a valid CAS Registry Number.
108574-73-8Relevant articles and documents
Reduction of Nitroarenes to Anilines in Basic Alcoholic Media
Prato, Maurizio,Quintily, Ugo,Scorrano, Gianfranco
, p. 1419 - 1424 (2007/10/02)
Substituted nitrobenzenes are reduced by alkoxide ions in alcohols to the corresponding azoxy and aniline derivatives.The reaction leading to anilines has been investigated in detail.Two different processes have been identified, both initiated by the condensation between the nitrosoarene intermediate (the first product of the reduction reaction) and the product of oxidation of the solvent.The imino derivative thus formed (ArN=CH-COR) may either undergo hydrolysis (to aniline) or form, through a series of redox processes, compounds containing the ArNH-CO moiety.These are also hydrolysed to anilines in a slower reaction.
