31912-08-0 Usage
General Description
(2-chloro-6-nitrophenyl)acetic acid, also known as 2-chloro-6-nitrobenzeneacetic acid, is a chemical compound with the molecular formula C8H6ClNO4. It is a derivative of acetic acid, with a nitro group and a chlorine atom attached to a phenyl ring. (2-chloro-6-nitrophenyl)acetic acid is commonly used in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It has also been studied for its potential use as an antimicrobial and anticancer agent. Additionally, (2-chloro-6-nitrophenyl)acetic acid is a halogenated aromatic compound, which means it can have potential environmental and health impacts if not handled and disposed of properly.
Check Digit Verification of cas no
The CAS Registry Mumber 31912-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,1 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 31912-08:
(7*3)+(6*1)+(5*9)+(4*1)+(3*2)+(2*0)+(1*8)=90
90 % 10 = 0
So 31912-08-0 is a valid CAS Registry Number.
31912-08-0Relevant articles and documents
Synthesis and diuretic activity of 4,5-dihydro-6H-imidazo[4,5,1- ij]quinoline-6-one 6-oxime-O-sulfonic acid derivatives
Nishijima, Kazumi,Shinkawa, Tomoaki,Ito, Manabu,Nishida, Hidemitsu,Yamamoto, Ichirou,Onuki, Yoshiaki,Inaba, Hitoshi,Miyano, Soutarou
, p. 763 - 774 (2007/10/03)
Using our previously reported 7-chloro-2,3-dihydro-1-(2-methylbenzoyl)- 4(1H)-quinolinone 4-oxime-O-sulfonic acid potassium salt la (M17055) as a lead, a series of tricyclic (2a-o, 3, 4, 5) and tetracyclic (6) quinolinone oxime O-sulfonic acid derivatives were synthesized by ring annulation of the 1-(2-methylbenzoyl) moiety to the quinolinone skeleton. They were compared with furosemide and compound 1a for diuretic activity in dogs; some tricyclic 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one 6-oxime-O-sulfonic acid derivatives showed diuretic activity comparable (2c,e) or superior (2m) to the lead compound 1a. These results are discussed on the basis of a comparison of the conformational and electronic characteristics of the relevant compounds with the aid of computer graphics.