Cas 112378-27-5,2-Benzoyl-1-methoxycarbonylmethyl-9-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester

112378-27-5

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Basic information

Product Name: 2-Benzoyl-1-methoxycarbonylmethyl-9-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester
Synonyms: 2-Benzoyl-1-methoxycarbonylmethyl-9-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester
CAS NO:112378-27-5
Molecular Formula:
Molecular Weight: 420.465
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: 2-Benzoyl-1-methoxycarbonylmethyl-9-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Benzoyl-1-methoxycarbonylmethyl-9-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(112378-27-5)
EPA Substance Registry System: 2-Benzoyl-1-methoxycarbonylmethyl-9-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(112378-27-5)

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: 112378-27-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112378-27-5 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, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112378-27:
(8*1)+(7*1)+(6*2)+(5*3)+(4*7)+(3*8)+(2*2)+(1*7)=105
105 % 10 = 5
So 112378-27-5 is a valid CAS Registry Number.

112378-27-5Upstream product

7303-49-3 DL-tryptophan methyl ester

112378-27-5Downstream Products

112378-19-5 (E)-3-[3-(2-Benzoylamino-2-methoxycarbonyl-ethyl)-1-methyl-1H-indol-2-yl]-acrylic acid methyl ester

112378-27-5Relevant 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 (1987)

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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