Cas 938186-07-3,(αS)-α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-N,N-dimethyl-1H-indole-4-propanamide

938186-07-3

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Basic information

Product Name: (αS)-α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-N,N-dimethyl-1H-indole-4-propanamide
Synonyms: (αS)-α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-N,N-dimethyl-1H-indole-4-propanamide
CAS NO:938186-07-3
Molecular Formula:
Molecular Weight: 465.549
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: (αS)-α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-N,N-dimethyl-1H-indole-4-propanamide(CAS DataBase Reference)
NIST Chemistry Reference: (αS)-α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-N,N-dimethyl-1H-indole-4-propanamide(938186-07-3)
EPA Substance Registry System: (αS)-α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-N,N-dimethyl-1H-indole-4-propanamide(938186-07-3)

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: 938186-07-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 938186-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,8,1,8 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 938186-07:
(8*9)+(7*3)+(6*8)+(5*1)+(4*8)+(3*6)+(2*0)+(1*7)=203
203 % 10 = 3
So 938186-07-3 is a valid CAS Registry Number.

938186-07-3Upstream product

460096-20-2 (S)-N^α-benzyloxycarbonyl-Nⁱⁿ-tert-butyloxycarbonyl-3-(indol-4'-yl)-alanine, methyl ester

938186-07-3Downstream Products

938186-10-8 (αS)-α-{[(benzyloxy)carbonyl]amino}-N,N-dimethyl-1H-indole-4-propanamide

938186-07-3Relevant academic research and scientific papers

Model construction for the A-B-C ring system of lysergic acid via Vilsmeier-Haack-type cyclization of 1H-indole-4-propanoic acid derivatives

Kurokawa, Masayuki,Watanabe, Toshiko,Ishikawa, Tsutomu

, p. 574 - 587 (2008/02/07)

Vilsmeier-Haack-type cyclization of 1H-indole-4-propanoic acid derivatives was examined as model construction for the A-B-C ring system of lysergic acid (1). Smooth cyclization from the 4 position of 1H-indole to the 3 position was achieved by Vilsmeier-H

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