77223-21-3 Usage
General Description
7-CHLORO-2,4-DIMETHYL-[1,8]NAPHTHYRIDINE is a chemical compound with a naphthyridine structure that contains a chloro and two methyl groups. It is used in the pharmaceutical industry as a building block for the synthesis of various drug compounds. This chemical exhibits potent antimicrobial and anti-inflammatory properties, making it a valuable ingredient in the development of new medications for the treatment of infections and inflammatory conditions. Additionally, 7-CHLORO-2,4-DIMETHYL-[1,8]NAPHTHYRIDINE may also have potential applications in agricultural and veterinary products as a pesticide or antibacterial agent. Its unique structure and functional properties make it a versatile and important chemical in the fields of medicine and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 77223-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,2 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77223-21:
(7*7)+(6*7)+(5*2)+(4*2)+(3*3)+(2*2)+(1*1)=123
123 % 10 = 3
So 77223-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClN2/c1-6-5-7(2)12-10-8(6)3-4-9(11)13-10/h3-5H,1-2H3
77223-21-3Relevant articles and documents
1,8-naphthyridine modified naphthalimide derivative: Ratiometric and selective sensor for hg2+ in organic aqueous solution
Shi, Yong Gang,Duan, Yu Lian,Chen, Jian Hua,Wu, Xiang Hua,Zhou, Ying,Zhang, Jun Feng
, p. 63 - 67 (2013)
A bottom-modified (4-position) naphthalimide derivative 1 with 1,8-naphthyridine as binding site has been designed and synthesized. Compound 1 is the first 1,8-naphthyridine-modified naphthalimide-based sensor that can detect Hghg2+ selectively with respect to ratiometric fluorescent change and blue shift in organic aqueous solution. The Job's plot and FAB mass indicate that 1 formed a 1:1 complex with Hg2+. A top-modified naphthalimide derivative 2 with 1,8-naphthyridin as binding site has also been synthesized for comparison.
Substituted 1,8-naphthyridines, their preparation and their use as antidotes
-
, (2008/06/13)
A combination of a variety of herbicides with safening agents which are substituted 1,8-naphthyridines of the formula STR1 where R1 is mercapto, hydroxyl, halogen, benzylthio, amino or NR2 R3, where R2 is a grou