Cas 1314307-52-2,ethyl 2-(3-formyl-8-methylquinolin-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate

1314307-52-2

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Basic information

Product Name: ethyl 2-(3-formyl-8-methylquinolin-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate
Synonyms: ethyl 2-(3-formyl-8-methylquinolin-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate
CAS NO:1314307-52-2
Molecular Formula:
Molecular Weight: 326.309
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl 2-(3-formyl-8-methylquinolin-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(3-formyl-8-methylquinolin-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate(1314307-52-2)
EPA Substance Registry System: ethyl 2-(3-formyl-8-methylquinolin-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate(1314307-52-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1314307-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1314307-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,3,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1314307-52:
(9*1)+(8*3)+(7*1)+(6*4)+(5*3)+(4*0)+(3*7)+(2*5)+(1*2)=112
112 % 10 = 2
So 1314307-52-2 is a valid CAS Registry Number.

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1314307-52-2Relevant academic research and scientific papers

Facile synthesis of some new pyrimidoquinolines

Marjani, Ahmad Poursattar,Khalafy, Jabbar,Ebrahimlo, Ali Reza Molla

experimental part, p. 2475 - 2482 (2011/08/05)

The reaction of ethyl 5-oxo-2,5-dihydroisoxzole-4-carboxylate with derivatives of 2-chloroquinoline afforded the desired N-quinolinyl isoxazolones. Their reactions with triethylamine in chloroform produced the corresponding pyrimidoquinoline derivatives, through intramolecular cyclization.

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