Cas 118404-38-9,[(S)-2-(3-Methyl-butyrylamino)-3-phenyl-propylsulfanyl]-acetic acid

118404-38-9

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Basic information

Product Name: [(S)-2-(3-Methyl-butyrylamino)-3-phenyl-propylsulfanyl]-acetic acid
Synonyms: [(S)-2-(3-Methyl-butyrylamino)-3-phenyl-propylsulfanyl]-acetic acid
CAS NO:118404-38-9
Molecular Formula:
Molecular Weight: 309.43
EINECS: N/A
Product Categories: N/A
Mol File: 118404-38-9.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: [(S)-2-(3-Methyl-butyrylamino)-3-phenyl-propylsulfanyl]-acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-2-(3-Methyl-butyrylamino)-3-phenyl-propylsulfanyl]-acetic acid(118404-38-9)
EPA Substance Registry System: [(S)-2-(3-Methyl-butyrylamino)-3-phenyl-propylsulfanyl]-acetic acid(118404-38-9)

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: 118404-38-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118404-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,4,0 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 118404-38:
(8*1)+(7*1)+(6*8)+(5*4)+(4*0)+(3*4)+(2*3)+(1*8)=109
109 % 10 = 9
So 118404-38-9 is a valid CAS Registry Number.

118404-38-9Upstream product

118404-38-9Downstream Products

124339-15-7 Iva-PheΨGly-Sta-Leu-NHCH2Ph

118404-38-9Relevant articles and documents

Renin inhibitors containing isosteric replacements of the amide bond connecting the P3 and P2 sites

Kaltenbronn,Hudspeth,Lunney,Michniewicz,Nicolaides,Repine,Roark,Stier,Tinney,Woo,Essenburg

, p. 838 - 845 (2007/10/02)

Renin inhibitors having 13 different isosteres connecting the P3 and P2 positions have been prepared. Synthetic routes and in vitro activity exhibited by these compounds are discussed. The two most potent compounds, 47 and 48, contai

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