Cas 861213-75-4,rac-2-amino-3-{[4-(2-ethylphenyl)-1H-indole-2-carbonyl]amino}propionic acid

861213-75-4

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Basic information

Product Name: rac-2-amino-3-{[4-(2-ethylphenyl)-1H-indole-2-carbonyl]amino}propionic acid
Synonyms: rac-2-amino-3-{[4-(2-ethylphenyl)-1H-indole-2-carbonyl]amino}propionic acid
CAS NO:861213-75-4
Molecular Formula:
Molecular Weight: 351.405
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: rac-2-amino-3-{[4-(2-ethylphenyl)-1H-indole-2-carbonyl]amino}propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: rac-2-amino-3-{[4-(2-ethylphenyl)-1H-indole-2-carbonyl]amino}propionic acid(861213-75-4)
EPA Substance Registry System: rac-2-amino-3-{[4-(2-ethylphenyl)-1H-indole-2-carbonyl]amino}propionic acid(861213-75-4)

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: 861213-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 861213-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,2,1 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 861213-75:
(8*8)+(7*6)+(6*1)+(5*2)+(4*1)+(3*3)+(2*7)+(1*5)=154
154 % 10 = 4
So 861213-75-4 is a valid CAS Registry Number.

861213-75-4Upstream product

1210054-71-9 C₂₈H₂₇N₃O₅

861213-75-4Downstream Products

861213-75-4Relevant academic research and scientific papers

Drug design, in vitro pharmacology, and structure-activity relationships of 3-acylamino-2-aminopropionic acid derivatives, a novel class of partial agonists at the glycine site on the N-methyl-D-aspartate (NMDA) receptor complex

Urwyler, Stephan,Floersheim, Philipp,Roy, Bernard L.,Koller, Manuel

experimental part, p. 5093 - 5107 (2010/03/02)

Retaining agonistic activity at the glycine coagonist site of the NMDA receptor in molecules derived from glycine or D-serine has proven to be difficult because in the vicinity of the α-amino acid group little substitution is tolerated. We have solved thi

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