Cas 127627-93-4,(1S,3S)-Methyl 2-<2-(benzyloxycarbonyl)-S-prolyl>-1-(2-oxopropyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-3-carboxylate

127627-93-4

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Basic information

Product Name: (1S,3S)-Methyl 2-<2-(benzyloxycarbonyl)-S-prolyl>-1-(2-oxopropyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-3-carboxylate
Synonyms: (1S,3S)-Methyl 2-<2-(benzyloxycarbonyl)-S-prolyl>-1-(2-oxopropyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-3-carboxylate
CAS NO:127627-93-4
Molecular Formula:
Molecular Weight: 517.582
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: (1S,3S)-Methyl 2-<2-(benzyloxycarbonyl)-S-prolyl>-1-(2-oxopropyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3S)-Methyl 2-<2-(benzyloxycarbonyl)-S-prolyl>-1-(2-oxopropyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-3-carboxylate(127627-93-4)
EPA Substance Registry System: (1S,3S)-Methyl 2-<2-(benzyloxycarbonyl)-S-prolyl>-1-(2-oxopropyl)-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-3-carboxylate(127627-93-4)

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: 127627-93-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127627-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,2 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127627-93:
(8*1)+(7*2)+(6*7)+(5*6)+(4*2)+(3*7)+(2*9)+(1*3)=144
144 % 10 = 4
So 127627-93-4 is a valid CAS Registry Number.

127627-93-4Upstream product

127627-93-4Downstream Products

106211-91-0 Demethoxyfumitremorgin C

127627-93-4Relevant academic research and scientific papers

An Asymmetric Route to the Demethoxy-fumitremorgins

Bailey, Patrick D.,Hollinshead, Sean P.,McLay, Neil R.,Everett, Judith H.,Reynolds, Colin D.,et al.

, p. 451 - 458 (2007/10/02)

By use of a modified Pictet-Spengler reaction under conditions of kinetic control, the optically pure cis-1,3-disubstituted tetrahydro-β-carboline 21a was prepared from L-tryptophan; this generated a key tricyclic unit that possessed the correct relative

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