Cas 90787-06-7,ethyl 4-(4-methoxyphenyl)-1,2-dimethyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate

90787-06-7

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Basic information

Product Name: ethyl 4-(4-methoxyphenyl)-1,2-dimethyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate
Synonyms: ethyl 4-(4-methoxyphenyl)-1,2-dimethyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate
CAS NO:90787-06-7
Molecular Formula: C24H23NO4
Molecular Weight: 389.44372
EINECS: N/A
Product Categories: N/A
Mol File: 90787-06-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl 4-(4-methoxyphenyl)-1,2-dimethyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-(4-methoxyphenyl)-1,2-dimethyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate(90787-06-7)
EPA Substance Registry System: ethyl 4-(4-methoxyphenyl)-1,2-dimethyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate(90787-06-7)

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: 90787-06-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90787-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,8 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90787-06:
(7*9)+(6*0)+(5*7)+(4*8)+(3*7)+(2*0)+(1*6)=157
157 % 10 = 7
So 90787-06-7 is a valid CAS Registry Number.

90787-06-7Upstream product

90787-06-7Downstream Products

90787-06-7Relevant academic research and scientific papers

C- AND N-ALKYLATION OF 4,5-DIHYDRO-1H-INDENOPYRIDINE DERIVATIVES

Lusis, V. K.,Mutsenietse, D. Kh.,Zandersons, A. Z.,Mazheika, I. B.,Dubur, G. Ya.

, p. 318 - 323 (2007/10/02)

2-Methyl-4-aryl-5-oxo-4,5-dihydro-1H-indenopyridine derivatives react with methyl iodide in an aprotic medium in the presence of alkaline agents to give C- and N-alkylation products, viz., 2,4a-dimethyl- and 1,2-dimethyl-4-aryl-5-oxo-4,5-dihydroind

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