Cas 123482-72-4,(S)-2-[(2R,3S)-3-tert-Butoxycarbonylamino-2-(tert-butyl-dimethyl-silanyloxy)-4-phenyl-butyl]-hept-6-enoic acid

123482-72-4

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Basic information

Product Name: (S)-2-[(2R,3S)-3-tert-Butoxycarbonylamino-2-(tert-butyl-dimethyl-silanyloxy)-4-phenyl-butyl]-hept-6-enoic acid
Synonyms: (S)-2-[(2R,3S)-3-tert-Butoxycarbonylamino-2-(tert-butyl-dimethyl-silanyloxy)-4-phenyl-butyl]-hept-6-enoic acid
CAS NO:123482-72-4
Molecular Formula:
Molecular Weight: 505.77
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)-2-[(2R,3S)-3-tert-Butoxycarbonylamino-2-(tert-butyl-dimethyl-silanyloxy)-4-phenyl-butyl]-hept-6-enoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(2R,3S)-3-tert-Butoxycarbonylamino-2-(tert-butyl-dimethyl-silanyloxy)-4-phenyl-butyl]-hept-6-enoic acid(123482-72-4)
EPA Substance Registry System: (S)-2-[(2R,3S)-3-tert-Butoxycarbonylamino-2-(tert-butyl-dimethyl-silanyloxy)-4-phenyl-butyl]-hept-6-enoic acid(123482-72-4)

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: 123482-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123482-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123482-72:
(8*1)+(7*2)+(6*3)+(5*4)+(4*8)+(3*2)+(2*7)+(1*2)=114
114 % 10 = 4
So 123482-72-4 is a valid CAS Registry Number.

123482-72-4Upstream product

123482-72-4Downstream Products

123411-33-6 [(1S,2R,4S)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-((1S,2S)-1-cyclohexylmethyl-2-hydroxy-4-isobutylcarbamoyl-pent-4-enylcarbamoyl)-non-8-enyl]-carbamic acid tert-butyl ester

123482-72-4Relevant academic research and scientific papers

Renin inhibitors based on dipeptide analogues. Incorporation of the hydroxyethylene isostere at the P2/P3 sites

Kempf,De Lara,Stein,Cohen,Egan,Plattner

, p. 371 - 374 (2007/10/02)

The synthesis of a series of renin inhibitors in which the P2 and P3 amino acids are replaced with the hydroxyethylene dipeptide isostere is reported. In vitro evaluation of the inhibitors has revealed that this isostere is an accept

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