Cas 118586-64-4,{(S)-1-[(S)-1-((1S,2S,4R)-2,6-Dihydroxy-1-isobutyl-4-isobutylcarbamoyl-hexylcarbamoyl)-pentylcarbamoyl]-2-naphthalen-1-yl-ethyl}-carbamic acid benzyl ester

118586-64-4

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Basic information

Product Name: {(S)-1-[(S)-1-((1S,2S,4R)-2,6-Dihydroxy-1-isobutyl-4-isobutylcarbamoyl-hexylcarbamoyl)-pentylcarbamoyl]-2-naphthalen-1-yl-ethyl}-carbamic acid benzyl ester
Synonyms:
CAS NO:118586-64-4
Molecular Formula:
Molecular Weight: 732.961
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)-1-[(S)-1-((1S,2S,4R)-2,6-Dihydroxy-1-isobutyl-4-isobutylcarbamoyl-hexylcarbamoyl)-pentylcarbamoyl]-2-naphthalen-1-yl-ethyl}-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(S)-1-[(S)-1-((1S,2S,4R)-2,6-Dihydroxy-1-isobutyl-4-isobutylcarbamoyl-hexylcarbamoyl)-pentylcarbamoyl]-2-naphthalen-1-yl-ethyl}-carbamic acid benzyl ester(118586-64-4)
EPA Substance Registry System: {(S)-1-[(S)-1-((1S,2S,4R)-2,6-Dihydroxy-1-isobutyl-4-isobutylcarbamoyl-hexylcarbamoyl)-pentylcarbamoyl]-2-naphthalen-1-yl-ethyl}-carbamic acid benzyl ester(118586-64-4)

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: 118586-64-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118586-64-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118586-64:
(8*1)+(7*1)+(6*8)+(5*5)+(4*8)+(3*6)+(2*6)+(1*4)=154
154 % 10 = 4
So 118586-64-4 is a valid CAS Registry Number.

118586-64-4Upstream product

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118586-64-4Relevant academic research and scientific papers

Renin inhibitors. I. Synthesis and structure-activity relationship of transition-state inhibitors containing homostatine analogues at the scissile bond

Atsuumi,Nakano,Koike,Tanake,Matsuyama,Nakano,Morishima

, p. 364 - 370 (2007/10/02)

The synthesis and structure-activity relationships of transition-state renin inhibitors containing the homostatine analogues at the scissile bond are described. These inhibitors incorporate the amino acid side chains corresponding to positions 7-12 (Psub

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