85126-67-6 Usage
Description
4-(2-Chloro-acetylamino)-benzamide is a chemical compound with a molecular formula C9H8ClNO2. It is a type of benzamide derivative, containing a benzene ring with an amide group and a chlorine atom. 4-(2-Chloro-acetylamino)-benzamide is commonly used in pharmaceutical research and development due to its potential to exhibit various biological activities.
Uses
Used in Pharmaceutical Research and Development:
4-(2-Chloro-acetylamino)-benzamide is used as a potential inhibitor of certain enzymes for its ability to interact with biological targets, making it a candidate for the development of new drugs.
Used in Drug Target Identification:
4-(2-Chloro-acetylamino)-benzamide serves as a potential drug target for the treatment of certain diseases, given its capacity to modulate specific biological pathways or processes.
Used in Dyes and Pigments Production:
Due to its chemical structure, 4-(2-Chloro-acetylamino)-benzamide may also have applications in the production of dyes and pigments, where its unique properties can contribute to the coloration and stability of these products.
Further research and testing are necessary to fully understand the properties and applications of 4-(2-Chloro-acetylamino)-benzamide, ensuring its safe and effective use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 85126-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,2 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85126-67:
(7*8)+(6*5)+(5*1)+(4*2)+(3*6)+(2*6)+(1*7)=136
136 % 10 = 6
So 85126-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClN2O2/c10-5-8(13)12-7-3-1-6(2-4-7)9(11)14/h1-4H,5H2,(H2,11,14)(H,12,13)
85126-67-6Relevant articles and documents
Synthesis of α-chloroamides in water
Harte, Andrew J.,Gunnlaugsson, Thorfinnur
, p. 6321 - 6324 (2007/10/03)
The reaction between chloroacetyl chloride and mono- or bis-aliphatic or aromatic amines in water under basic or neutral conditions gives rise to the formation of a variety of functionalized α-chloroamides. The resulting products were obtained as solids in moderate to good yields, upon precipitation and isolation by filtration.
