Cas 159142-00-4,(R)-N-(1S,2R)-<3-<2-<<(1,1-dimethylethyl)amino>carbonyl>phenyl>-2-hydroxy-1-(phenylmethyl)propyl>-2-amino-4-oxo-4-(benzyloxy)butanamide

159142-00-4

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Basic information

Product Name: (R)-N-(1S,2R)-<3-<2-<<(1,1-dimethylethyl)amino>carbonyl>phenyl>-2-hydroxy-1-(phenylmethyl)propyl>-2-amino-4-oxo-4-(benzyloxy)butanamide
Synonyms: (R)-N-(1S,2R)-<3-<2-<<(1,1-dimethylethyl)amino>carbonyl>phenyl>-2-hydroxy-1-(phenylmethyl)propyl>-2-amino-4-oxo-4-(benzyloxy)butanamide
CAS NO:159142-00-4
Molecular Formula:
Molecular Weight: 545.679
EINECS: N/A
Product Categories: N/A
Mol File: 159142-00-4.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: (R)-N-(1S,2R)-<3-<2-<<(1,1-dimethylethyl)amino>carbonyl>phenyl>-2-hydroxy-1-(phenylmethyl)propyl>-2-amino-4-oxo-4-(benzyloxy)butanamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-(1S,2R)-<3-<2-<<(1,1-dimethylethyl)amino>carbonyl>phenyl>-2-hydroxy-1-(phenylmethyl)propyl>-2-amino-4-oxo-4-(benzyloxy)butanamide(159142-00-4)
EPA Substance Registry System: (R)-N-(1S,2R)-<3-<2-<<(1,1-dimethylethyl)amino>carbonyl>phenyl>-2-hydroxy-1-(phenylmethyl)propyl>-2-amino-4-oxo-4-(benzyloxy)butanamide(159142-00-4)

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: 159142-00-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 159142-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,1,4 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 159142-00:
(8*1)+(7*5)+(6*9)+(5*1)+(4*4)+(3*2)+(2*0)+(1*0)=124
124 % 10 = 4
So 159142-00-4 is a valid CAS Registry Number.

159142-00-4Upstream product

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159142-00-4Relevant articles and documents

Potent human immunodeficiency virus type 1 protease inhibitors that utilize noncoded D-amino acids as P2/P3 ligands

Jungheim, Louis N.,Shepherd, Timothy A.,Baxter, Angela J.,Burgess, Jeffrey,Hatch, Steven D.,Lubbehusen, Penny,Wiskerchen, MaryAnn,Muesing, Mark A.

, p. 96 - 108 (1996)

Noncoded D-amino acids have been designed to replace the quinaldic amide- asparaginyl moiety (P2/P3 ligand) found in several potent human immunodeficiency virus (HIV) protease inhibitors such as LY289612. The substituted nitrogen, op

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