Cas 295321-65-2,(S)-2-Amino-N-{(S)-3-[(S)-2-amino-3-(4-amino-phenyl)-propionylamino]-1-hydroxymethyl-propyl}-3-(4-amino-phenyl)-propionamide

295321-65-2

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Basic information

Product Name: (S)-2-Amino-N-{(S)-3-[(S)-2-amino-3-(4-amino-phenyl)-propionylamino]-1-hydroxymethyl-propyl}-3-(4-amino-phenyl)-propionamide
Synonyms: (S)-2-Amino-N-{(S)-3-[(S)-2-amino-3-(4-amino-phenyl)-propionylamino]-1-hydroxymethyl-propyl}-3-(4-amino-phenyl)-propionamide
CAS NO:295321-65-2
Molecular Formula:
Molecular Weight: 428.534
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-Amino-N-{(S)-3-[(S)-2-amino-3-(4-amino-phenyl)-propionylamino]-1-hydroxymethyl-propyl}-3-(4-amino-phenyl)-propionamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-Amino-N-{(S)-3-[(S)-2-amino-3-(4-amino-phenyl)-propionylamino]-1-hydroxymethyl-propyl}-3-(4-amino-phenyl)-propionamide(295321-65-2)
EPA Substance Registry System: (S)-2-Amino-N-{(S)-3-[(S)-2-amino-3-(4-amino-phenyl)-propionylamino]-1-hydroxymethyl-propyl}-3-(4-amino-phenyl)-propionamide(295321-65-2)

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: 295321-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 295321-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,5,3,2 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 295321-65:
(8*2)+(7*9)+(6*5)+(5*3)+(4*2)+(3*1)+(2*6)+(1*5)=152
152 % 10 = 2
So 295321-65-2 is a valid CAS Registry Number.

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295321-65-2Relevant academic research and scientific papers

Synthesis and activity of new acylated diaminohydroxyalkanes as human immunodeficiency virus protease inhibitors

Marastoni, Mauro,Bazzaro, Martina,Bortolotti, Fabrizio,Tomatis, Roberto

, p. 564 - 568 (2007/10/03)

A series of HIV-1 protease inhibitors based on the lead compound Pc (IC50 = 165 nmol/l) with structural modifications at P1/P1' substituents or with a lengthening at its core unit were synthesized from amino acid starting materials. All analogu

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