115175-22-9 Usage
General Description
3-Amino-3'-chlorobenzanilide, also known as N-(3-amino-4-chlorophenyl)benzamide, is a chemical compound with the molecular formula C13H11ClN2O. It is a white to off-white crystalline powder that is primarily used as an intermediate in the pharmaceutical industry for the synthesis of various drugs and active pharmaceutical ingredients. 3-AMINO-3'-CHLOROBENZANILIDE has also been studied for its potential anti-inflammatory and analgesic properties. Additionally, 3-Amino-3'-chlorobenzanilide has been used in research as a building block for the synthesis of novel organic molecules with biological activity. Overall, this compound plays a vital role in the development of pharmaceuticals and has potential applications in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 115175-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,7 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115175-22:
(8*1)+(7*1)+(6*5)+(5*1)+(4*7)+(3*5)+(2*2)+(1*2)=99
99 % 10 = 9
So 115175-22-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H11ClN2O/c14-10-4-2-6-12(8-10)16-13(17)9-3-1-5-11(15)7-9/h1-8H,15H2,(H,16,17)
115175-22-9Relevant articles and documents
Synthesis and Antiviral Activity of Sulfonamidobenzophenone Oximes and Sulfonamidobenzamides
Ogata, Masaru,Matsumoto, Hiroshi,Shimizu, Sumio,Kida, Shiro,Wada, Toru,et al.
, p. 417 - 423 (2007/10/02)
To find antiviral agents, various sulfonamidobenzophenone oximes (II) were synthesized from the appropriate m-sulfonamidobenzophenones by hydroxylamine reaction.The reaction products were generally obtained as syn/anti mixtures which were separable by fractional crystallization.The anti isomer had more potent antipoliovirus activity than the syn isomer.Various sulfonamidobenzamides (III) which were structurally related to II were synthesized by the reaction of amino-substituted benzamides with sulfuryl chloride or amines with (aminosulfonyl)benzoyl chloride.Antiviral activity was examined by the plaque-inhibition test.Compounds 5, 36, and 69 exhibited strong antipicornavirus activity.The structure-activity relationships are discussed.
