Cas 552336-93-3,butyl 3-(4-methylphenyl)amino-2-(5-nitropyrid-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate

552336-93-3

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Basic information

Product Name: butyl 3-(4-methylphenyl)amino-2-(5-nitropyrid-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate
Synonyms: butyl 3-(4-methylphenyl)amino-2-(5-nitropyrid-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate
CAS NO:552336-93-3
Molecular Formula:
Molecular Weight: 412.402
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: butyl 3-(4-methylphenyl)amino-2-(5-nitropyrid-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: butyl 3-(4-methylphenyl)amino-2-(5-nitropyrid-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate(552336-93-3)
EPA Substance Registry System: butyl 3-(4-methylphenyl)amino-2-(5-nitropyrid-2-yl)-5-oxo-2,5-dihydroisoxazole-4-carboxylate(552336-93-3)

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: 552336-93-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 552336-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,2,3,3 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 552336-93:
(8*5)+(7*5)+(6*2)+(5*3)+(4*3)+(3*6)+(2*9)+(1*3)=153
153 % 10 = 3
So 552336-93-3 is a valid CAS Registry Number.

552336-93-3Upstream product

552336-93-3Downstream Products

552336-93-3Relevant academic research and scientific papers

Synthesis of 2-(5-nitropyrid-2-yl)-3-(4-substitutedphenyl)aminoisoxazol- 5(2h)-ones and their rearrangements to imidazo[1,2-a]-pyridines and indoles with triethylamine

Khalafy,Setamdideh,Dilmaghani, K. Akbari

, p. 907 - 916 (2002)

3-(4-Substitutedphenyl)aminoisoxazol-5(2H)-ones, substituted on nitrogen with a nitropyridine group, react with triethylamine to give imidazo[1,2-a]pyridines and indoles. With 4-bromophenyl and 4-methylphenyl group substituents only imidazopyridines are f

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