Cas 68014-42-6,2-benzyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-9-methyl-pyrido-<3,4b>indole-1-(3-pentanone)

68014-42-6

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Basic information

Product Name: 2-benzyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-9-methyl-pyrido-<3,4b>indole-1-(3-pentanone)
Synonyms:
CAS NO:68014-42-6
Molecular Formula:
Molecular Weight: 418.536
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: 2-benzyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-9-methyl-pyrido-<3,4b>indole-1-(3-pentanone)(CAS DataBase Reference)
NIST Chemistry Reference: 2-benzyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-9-methyl-pyrido-<3,4b>indole-1-(3-pentanone)(68014-42-6)
EPA Substance Registry System: 2-benzyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-9-methyl-pyrido-<3,4b>indole-1-(3-pentanone)(68014-42-6)

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: 68014-42-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 68014-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,1 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68014-42:
(7*6)+(6*8)+(5*0)+(4*1)+(3*4)+(2*4)+(1*2)=116
116 % 10 = 6
So 68014-42-6 is a valid CAS Registry Number.

68014-42-6Upstream product

68014-42-6Downstream Products

141804-37-7 5-methyl-8-propionyl-9-oxo-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctindole

68014-42-6Relevant academic research and scientific papers

Pictet-Spengler reactions in aprotic media. The total synthesis of (±) suaveoline

Trudell,Soerens,Weber,Hutchins,Grubisha,Bennett,Cook

, p. 1805 - 1822 (1992)

The first total synthesis of the indole alkaloid (±)-suaveoline 1 (a macroline-related base and a member of the sarpagine/ajmaline class of alkaloids) was completed in a stereocontrolled fashion. The serial synthesis employed three intramolecular reaction

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