Cas 752212-90-1,9H-Pyrido[3,4-b]indole-3-carboxylic acid, 9-[(pentafluorophenyl)methyl]-, ethyl ester

752212-90-1

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Basic information

Product Name: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 9-[(pentafluorophenyl)methyl]-, ethyl ester
Synonyms:
CAS NO:752212-90-1
Molecular Formula: C21H13F5N2O2
Molecular Weight: 420.338
EINECS: N/A
Product Categories: N/A
Mol File: 752212-90-1.mol
Article Data: 1

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: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 9-[(pentafluorophenyl)methyl]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 9-[(pentafluorophenyl)methyl]-, ethyl ester(752212-90-1)
EPA Substance Registry System: 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 9-[(pentafluorophenyl)methyl]-, ethyl ester(752212-90-1)

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: 752212-90-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 752212-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,2,2,1 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 752212-90:
(8*7)+(7*5)+(6*2)+(5*2)+(4*1)+(3*2)+(2*9)+(1*0)=141
141 % 10 = 1
So 752212-90-1 is a valid CAS Registry Number.

752212-90-1Upstream product

752212-90-1Downstream Products

752212-90-1Relevant articles and documents

Synthesis, acute toxicities, and antitumor effects of novel 9-substituted β-carboline derivatives

Cao, Rihui,Chen, Qi,Hou, Xuerui,Chen, Hongsheng,Guan, Huaji,Ma, Yan,Peng, Wenlie,Xu, Anlong

, p. 4613 - 4623 (2004)

A series of novel 9-substituted β-carboline derivatives was synthesized from the starting material harmine and l-tryptophan, respectively. Cytotoxic activities, acute toxicities, and antitumor effects of these compounds were investigated. A series of nove

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