Cas 1346787-36-7,(S)-methyl 2-(phenethylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate

1346787-36-7

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Basic information

Product Name: (S)-methyl 2-(phenethylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
Synonyms: (S)-methyl 2-(phenethylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
CAS NO:1346787-36-7
Molecular Formula:
Molecular Weight: 377.443
EINECS: N/A
Product Categories: N/A
Mol File: 1346787-36-7.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: (S)-methyl 2-(phenethylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-methyl 2-(phenethylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate(1346787-36-7)
EPA Substance Registry System: (S)-methyl 2-(phenethylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate(1346787-36-7)

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: 1346787-36-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1346787-36-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,7,8 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1346787-36:
(9*1)+(8*3)+(7*4)+(6*6)+(5*7)+(4*8)+(3*7)+(2*3)+(1*6)=197
197 % 10 = 7
So 1346787-36-7 is a valid CAS Registry Number.

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1346787-36-7Relevant articles and documents

Design, synthesis, and biological evaluation of callophycin A and analogues as potential chemopreventive and anticancer agents

Shen, Li,Park, Eun-Jung,Kondratyuk, Tamara P.,Guendisch, Daniela,Marler, Laura,Pezzuto, John M.,Wright, Anthony D.,Sun, Dianqing

, p. 6182 - 6195 (2011/12/15)

Callophycin A was originally isolated from the red aμgae Callophycus oppositifolius and shown to mediate anticancer and cytotoxic effects. In our collaborative effort to identify potential chemopreventive and anticancer agents with enhanced potency and se

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