Cas 112378-34-4,1H-Pyrido[3,4-b]indole-1-acetic acid, 2,3,4,9-tetrahydro-9-methyl-2-(1-oxo-3-phenyl-2-propenyl)-, methyl ester

112378-34-4

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Basic information

Product Name: 1H-Pyrido[3,4-b]indole-1-acetic acid, 2,3,4,9-tetrahydro-9-methyl-2-(1-oxo-3-phenyl-2-propenyl)-, methyl ester
Synonyms:
CAS NO:112378-34-4
Molecular Formula: C24H24N2O3
Molecular Weight: 388.466
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: 1H-Pyrido[3,4-b]indole-1-acetic acid, 2,3,4,9-tetrahydro-9-methyl-2-(1-oxo-3-phenyl-2-propenyl)-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Pyrido[3,4-b]indole-1-acetic acid, 2,3,4,9-tetrahydro-9-methyl-2-(1-oxo-3-phenyl-2-propenyl)-, methyl ester(112378-34-4)
EPA Substance Registry System: 1H-Pyrido[3,4-b]indole-1-acetic acid, 2,3,4,9-tetrahydro-9-methyl-2-(1-oxo-3-phenyl-2-propenyl)-, methyl ester(112378-34-4)

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: 112378-34-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112378-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,7 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112378-34:
(8*1)+(7*1)+(6*2)+(5*3)+(4*7)+(3*8)+(2*3)+(1*4)=104
104 % 10 = 4
So 112378-34-4 is a valid CAS Registry Number.

112378-34-4Upstream product

112378-34-4Downstream Products

112378-25-3 (E)-3-(1-Methyl-3-{2-[(E)-(3-phenyl-acryloyl)amino]-ethyl}-1H-indol-2-yl)-acrylic acid methyl ester

112378-34-4Relevant academic research and scientific papers

SYNTHESIS OF 3-(INDOL-2-YL)-PROPENOATE DERIVATIVES OF TRYPTAMINE, VALUABLE INTERMEDIATES FOR THE PREPARATION OF INDOLE ALKALOIDS

Bailey, Patrick D.,Hollinshead, Sean P.

, p. 2879 - 2882 (2007/10/02)

A simple three step route to 3-(indol-2-yl)-propenoate derivatives of tryptamine has been developed, involving the base-induced ring-opening of protected tetrahydro-β-carbolines that result from a modified Pictet-Spengler reaction.

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