6273-12-7 Usage
General Description
2-[[(2-Chlorophenyl)amino]carbonyl]-benzoic Acid is a complex aromatic compound, with one benzene ring substituted with a chloro group and an amino group, bonded to a carbonyl group which is further attached to another benzene ring substituted by a carboxylic acid group. 2-[[(2-CHLOROPHENYL)AMINO]CARBONYL]-BENZOIC ACID is known as an amide due to the presence of the carbonyl group (C=O) attached to a nitrogen atom. Its molecular formula is C14H10ClNO3. Chemical properties such as solubility, reactivity and stability of this compound would depend on the presence of these functional groups and their interactions with other chemicals or environmental factors. This chemical may be used in several chemical reactions or synthesis processes. However, potential applications and hazards related to this compound would require further investigation and validation.
Check Digit Verification of cas no
The CAS Registry Mumber 6273-12-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6273-12:
(6*6)+(5*2)+(4*7)+(3*3)+(2*1)+(1*2)=87
87 % 10 = 7
So 6273-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClNO3/c15-11-7-3-4-8-12(11)16-13(17)9-5-1-2-6-10(9)14(18)19/h1-8H,(H,16,17)(H,18,19)
6273-12-7Relevant articles and documents
Water mediated, environmentally friendly, step-wise, tandem & one-pot syntheses of 2-(1H-benzo[d]imidazole-2-yl)-N-arylbenzamides
Reddy, Yervala Dathu,Ramana Reddy, Chittireddy Venkata,Dubey, Pramod Kumar
, p. 2974 - 2979 (2014/01/06)
Water mediated and environmentally friendly, step-wise, tandem & one-pot syntheses of 2-(1H-benzo[d]imidazole-2-yl)-N-arylbenzamide derivatives have been developed by simply combining phthalic anhydride, anilines and phenylenediammonium dihydrogenphosphate. This reaction has an easy workup, provides excellent yields, and uses water as the solvent which is considered to be relatively environmentally benign.
Microwave assisted synthesis of N-Arylphthalamic acids with hyperlipidemic activity
Sena, Vera L.M,Srivastava, Rajendra M,Oliveira, Shalom P,Lima, Vera L.M
, p. 2671 - 2674 (2007/10/03)
A series of substituted N-arylphthalamic acids 3a-i has been synthesized by the reaction of phthalic anhydride 1 and aryl- or heterocyclic amines 2a-i, in the absence of solvents, in a domestic microwave oven. The formation of nine N-arylphthalamic acids was accomplished in 1-3 min giving excellent yields for compounds 3a-g, but moderate yield of compounds 3h and 3i, respectively. Compounds 3h and 3i are new. Interestingly, N-arylphthalamic acids 3a-i induced hyperlipidemia in Swiss white mice and also increased animals' body weight.
