Cas 869624-20-4,(S)-2-((R)-1-Cyano-2-phenyl-ethylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

869624-20-4

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Basic information

Product Name: (S)-2-((R)-1-Cyano-2-phenyl-ethylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester
Synonyms: (S)-2-((R)-1-Cyano-2-phenyl-ethylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester
CAS NO:869624-20-4
Molecular Formula:
Molecular Weight: 347.417
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: (S)-2-((R)-1-Cyano-2-phenyl-ethylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((R)-1-Cyano-2-phenyl-ethylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester(869624-20-4)
EPA Substance Registry System: (S)-2-((R)-1-Cyano-2-phenyl-ethylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester(869624-20-4)

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: 869624-20-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 869624-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,6,2 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 869624-20:
(8*8)+(7*6)+(6*9)+(5*6)+(4*2)+(3*4)+(2*2)+(1*0)=214
214 % 10 = 4
So 869624-20-4 is a valid CAS Registry Number.

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869624-20-4Relevant academic research and scientific papers

Novel domino cyclization of tryptophan-derived amino nitriles: Scope and stereoselectivity

Gonzalez-Vera, Juan A.,Garcia-Lopez, M. Teresa,Herranz, Rosario

, p. 8971 - 8976 (2005)

The scope and stereoselectivity of the acid-promoted cyclization of new tryptophan-based α-amino nitriles derived from either ketones or aldehydes to novel hexahydropyrrolo[1′,2′,3′:1,9a,9]imidazo-[1,2-a] indoles is described. This cyclization involves th

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