85152-74-5 Usage
Uses
Used in Pharmaceutical Industry:
[(4-chlorobenzyl)(nitroso)amino](phenyl)acetic acid can be used as an intermediate in the synthesis of various pharmaceutical compounds due to its diverse functional groups and structural complexity. The presence of the nitroso group may allow for the development of nitroxides with potential applications in drug design, particularly for targeting specific biological processes or receptors.
Used in Chemical Research:
In the field of chemical research, [(4-chlorobenzyl)(nitroso)amino](phenyl)acetic acid may serve as a starting material for the exploration of new reaction pathways and the synthesis of novel compounds with potential applications in various industries. Its unique structure could lead to the discovery of new chemical properties and reactivity patterns.
Used in Material Science:
[(4-chlorobenzyl)(nitroso)amino](phenyl)acetic acid's structural features may also make it a candidate for the development of new materials with specific properties in material science. For instance, its aromatic rings and functional groups could contribute to the creation of materials with tailored electronic, optical, or mechanical characteristics.
Used in Environmental Applications:
Given the presence of the carboxylic acid group, [(4-chlorobenzyl)(nitroso)amino](phenyl)acetic acid could potentially be utilized in environmental applications, such as in the development of new methods for pollutant removal or the creation of environmentally friendly materials.
Check Digit Verification of cas no
The CAS Registry Mumber 85152-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,5 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85152-74:
(7*8)+(6*5)+(5*1)+(4*5)+(3*2)+(2*7)+(1*4)=135
135 % 10 = 5
So 85152-74-5 is a valid CAS Registry Number.
85152-74-5Relevant articles and documents
Reaction of Sydnones with Oxygen
Nakajima, Masayuki,Anselme, Jean-Pierre
, p. 1444 - 1448 (2007/10/02)
The reaction of 3-benzyl- and 3-(p-chlorobenzyl)-4-phenylsydnones (1a and 1b) and of 3-benzylsydnone (1c) with oxygen at room temperature in the dark is described.Possible rationalizations for the formation of the products obtained are suggested.
