Cas 88238-74-8,1-(8-Benzyloxy-quinolin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester

88238-74-8

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Basic information

Product Name: 1-(8-Benzyloxy-quinolin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester
Synonyms:
CAS NO:88238-74-8
Molecular Formula:
Molecular Weight: 463.536
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: 1-(8-Benzyloxy-quinolin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-(8-Benzyloxy-quinolin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(88238-74-8)
EPA Substance Registry System: 1-(8-Benzyloxy-quinolin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(88238-74-8)

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: 88238-74-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88238-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,3 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88238-74:
(7*8)+(6*8)+(5*2)+(4*3)+(3*8)+(2*7)+(1*4)=168
168 % 10 = 8
So 88238-74-8 is a valid CAS Registry Number.

88238-74-8Upstream product

88238-74-8Downstream Products

88238-75-9 quinolyl-β-carboline

88238-74-8Relevant academic research and scientific papers

SYNTHETIC APPROACH TO THE ANTITUMOR ANTIBIOTIC LAVENDAMYCIN: A SYNTHESIS OF DEMETHYLLAVENDAMYCIN METHYL ESTER

Hibino, Satoshi,Okazaki, Miko,Sato, Kohichi,Morita, Itsuko,Ichikawa, Masataka

, p. 1957 - 1958 (2007/10/02)

A synthetic approach to the lavendamycin has been achieved by a formation of β-carboline derivative and oxidation of bromophenol derivative to the quinolinequinone system using cerium ammonium nitrate.

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