Cas 122334-64-9,(R)-2-[2-(1H-Indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester

122334-64-9

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Basic information

Product Name: (R)-2-[2-(1H-Indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester
Synonyms: (R)-2-[2-(1H-Indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester
CAS NO:122334-64-9
Molecular Formula:
Molecular Weight: 364.401
EINECS: N/A
Product Categories: N/A
Mol File: 122334-64-9.mol
Article Data: 1

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: (R)-2-[2-(1H-Indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-[2-(1H-Indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester(122334-64-9)
EPA Substance Registry System: (R)-2-[2-(1H-Indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid ethyl ester(122334-64-9)

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: 122334-64-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122334-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,3 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122334-64:
(8*1)+(7*2)+(6*2)+(5*3)+(4*3)+(3*4)+(2*6)+(1*4)=89
89 % 10 = 9
So 122334-64-9 is a valid CAS Registry Number.

122334-64-9Upstream product

122334-64-9Downstream Products

122334-79-6 (R)-2-[2-(1H-Indol-3-yl)-2-oxo-acetylamino]-3-phenyl-propionic acid

122334-64-9Relevant articles and documents

Specific Inhibition of Benzodiazepine Receptor Binding by Some N-(Indol-3-ylglyoxylyl)amino Acid Derivatives: Stereoselective Interactions

Primofiore, Giampaolo,Marini, Anna M.,Settimo, Federico Da,Martini, Claudia,Bardellini, Anna,et al.

, p. 2514 - 2518 (2007/10/02)

Several optically active N-(indolyl-3-ylglyoxylyl)amino acid derivatives were synthesized and tested for flunitrazepam displacing activity in bovine brain membranes.IC50 values were measured and revealed that the D form of the amino acid

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