Cas 141463-15-2,[(1S,2R)-1-Cyclohexylmethyl-2-hydroxy-3-(pyridin-2-ylsulfanyl)-propyl]-carbamic acid tert-butyl ester

141463-15-2

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Basic information

Product Name: [(1S,2R)-1-Cyclohexylmethyl-2-hydroxy-3-(pyridin-2-ylsulfanyl)-propyl]-carbamic acid tert-butyl ester
Synonyms: [(1S,2R)-1-Cyclohexylmethyl-2-hydroxy-3-(pyridin-2-ylsulfanyl)-propyl]-carbamic acid tert-butyl ester
CAS NO:141463-15-2
Molecular Formula:
Molecular Weight: 380.552
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-Cyclohexylmethyl-2-hydroxy-3-(pyridin-2-ylsulfanyl)-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(1S,2R)-1-Cyclohexylmethyl-2-hydroxy-3-(pyridin-2-ylsulfanyl)-propyl]-carbamic acid tert-butyl ester(141463-15-2)
EPA Substance Registry System: [(1S,2R)-1-Cyclohexylmethyl-2-hydroxy-3-(pyridin-2-ylsulfanyl)-propyl]-carbamic acid tert-butyl ester(141463-15-2)

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: 141463-15-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141463-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,4,6 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141463-15:
(8*1)+(7*4)+(6*1)+(5*4)+(4*6)+(3*3)+(2*1)+(1*5)=102
102 % 10 = 2
So 141463-15-2 is a valid CAS Registry Number.

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141463-15-2Relevant academic research and scientific papers

Renin inhibitors containing C-termini derived from mercaptoheterocycles

Ashton,Cantone,Meurer,Tolman,Greenlee,Patchett,Lynch,Schorn,Strouse,Siegl

, p. 2103 - 2112 (2007/10/02)

A series of transition-state analogues having heterocyclythio C-termini has been synthesized and evaluated for inhibition of human renin. Addition of mercaptoheterocycles to a chiral Boc-amino epoxide intermediate led, after several steps, to the target [

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