Cas 174174-73-3,[(1S,2R)-1-((R)-2-(1-Formyl-1H-indol-3-yl)-1-{(S)-1-[methyl-((S)-1-phenyl-ethyl)-carbamoyl]-2-phenyl-ethylcarbamoyl}-ethylcarbamoyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester

174174-73-3

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Basic information

Product Name: [(1S,2R)-1-((R)-2-(1-Formyl-1H-indol-3-yl)-1-{(S)-1-[methyl-((S)-1-phenyl-ethyl)-carbamoyl]-2-phenyl-ethylcarbamoyl}-ethylcarbamoyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester
Synonyms:
CAS NO:174174-73-3
Molecular Formula:
Molecular Weight: 697.831
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,2R)-1-((R)-2-(1-Formyl-1H-indol-3-yl)-1-{(S)-1-[methyl-((S)-1-phenyl-ethyl)-carbamoyl]-2-phenyl-ethylcarbamoyl}-ethylcarbamoyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(1S,2R)-1-((R)-2-(1-Formyl-1H-indol-3-yl)-1-{(S)-1-[methyl-((S)-1-phenyl-ethyl)-carbamoyl]-2-phenyl-ethylcarbamoyl}-ethylcarbamoyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester(174174-73-3)
EPA Substance Registry System: [(1S,2R)-1-((R)-2-(1-Formyl-1H-indol-3-yl)-1-{(S)-1-[methyl-((S)-1-phenyl-ethyl)-carbamoyl]-2-phenyl-ethylcarbamoyl}-ethylcarbamoyl)-2-hydroxy-propyl]-carbamic acid tert-butyl ester(174174-73-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 174174-73-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 174174-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,1,7 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 174174-73:
(8*1)+(7*7)+(6*4)+(5*1)+(4*7)+(3*4)+(2*7)+(1*3)=143
143 % 10 = 3
So 174174-73-3 is a valid CAS Registry Number.

174174-73-3Upstream product

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174174-73-3Relevant academic research and scientific papers

Synthesis and in vitro activities of highly potent and selective tripeptide antagonists of the neurokinin NK-1 receptor

Caliendo,Greco,Grieco,Perissutti,Santagada,Calignano,Mancuso,Novellino

, p. 755 - 759 (2007/10/03)

We report on the synthesis and the pharmacological properties of a new series of tachykinin antagonists based on the tripeptide Ac-Thr-D-Trp(CHO)-Phe-N(Me)-Bzl (1, FR113680) partly modified on the C-terminal amide part. Stereochemistry around the benzilic

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