Cas 96821-52-2,4-Oxo-1-p-tolyl-4,5-dihydro-1H-pyrido[3,2-b]indole-3-carboxylic acid ethyl ester

96821-52-2

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Basic information

Product Name: 4-Oxo-1-p-tolyl-4,5-dihydro-1H-pyrido[3,2-b]indole-3-carboxylic acid ethyl ester
Synonyms: 4-Oxo-1-p-tolyl-4,5-dihydro-1H-pyrido[3,2-b]indole-3-carboxylic acid ethyl ester
CAS NO:96821-52-2
Molecular Formula:
Molecular Weight: 346.386
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: 4-Oxo-1-p-tolyl-4,5-dihydro-1H-pyrido[3,2-b]indole-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Oxo-1-p-tolyl-4,5-dihydro-1H-pyrido[3,2-b]indole-3-carboxylic acid ethyl ester(96821-52-2)
EPA Substance Registry System: 4-Oxo-1-p-tolyl-4,5-dihydro-1H-pyrido[3,2-b]indole-3-carboxylic acid ethyl ester(96821-52-2)

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: 96821-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96821-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,2 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96821-52:
(7*9)+(6*6)+(5*8)+(4*2)+(3*1)+(2*5)+(1*2)=162
162 % 10 = 2
So 96821-52-2 is a valid CAS Registry Number.

96821-52-2Upstream product

84186-38-9 2-[1-[(1H-Indol-3-yl)-p-tolyl-amino]-meth-(Z)-ylidene]-malonic acid monoethyl ester

96821-52-2Downstream Products

96821-52-2Relevant academic research and scientific papers

TRANSITION FROM 3-INDOLECARBALDEHYDES TO 4-OXO-1,4-DIHYDRO-δ-CARBOLINES THROUGH α-(3-INDOLYL)-N-ARYLNITRONES

Yaroslavskii, I. S.,Velezheva, V. S.,Suvorov, N. N.

, p. 391 - 394 (2007/10/02)

α-(3-Indolyl)-N-arylnitrones, obtained from 3-indolecarbaldehydes and arylhydroxyamines, are converted by the action of sodiomalonic ester into N-aryl-N-(3-indolyl)-β-aminopropenoic esters.The latter are converted by the action of acetic or trifluoroaceti

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