Cas 447402-88-2,(S)-(tetrahydro-furan-3-yl) N-[3-[(4-amino-phenylsulfonyl)-isobutyl-amino]-2-oxo-1-phenylsulfanyl-propyl]-carbamate

447402-88-2

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Basic information

Product Name: (S)-(tetrahydro-furan-3-yl) N-[3-[(4-amino-phenylsulfonyl)-isobutyl-amino]-2-oxo-1-phenylsulfanyl-propyl]-carbamate
Synonyms: (S)-(tetrahydro-furan-3-yl) N-[3-[(4-amino-phenylsulfonyl)-isobutyl-amino]-2-oxo-1-phenylsulfanyl-propyl]-carbamate
CAS NO:447402-88-2
Molecular Formula:
Molecular Weight: 521.659
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)-(tetrahydro-furan-3-yl) N-[3-[(4-amino-phenylsulfonyl)-isobutyl-amino]-2-oxo-1-phenylsulfanyl-propyl]-carbamate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-(tetrahydro-furan-3-yl) N-[3-[(4-amino-phenylsulfonyl)-isobutyl-amino]-2-oxo-1-phenylsulfanyl-propyl]-carbamate(447402-88-2)
EPA Substance Registry System: (S)-(tetrahydro-furan-3-yl) N-[3-[(4-amino-phenylsulfonyl)-isobutyl-amino]-2-oxo-1-phenylsulfanyl-propyl]-carbamate(447402-88-2)

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: 447402-88-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 447402-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,7,4,0 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 447402-88:
(8*4)+(7*4)+(6*7)+(5*4)+(4*0)+(3*2)+(2*8)+(1*8)=152
152 % 10 = 2
So 447402-88-2 is a valid CAS Registry Number.

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447402-88-2Relevant academic research and scientific papers

Synthesis and antiviral activity of new anti-HIV amprenavir bioisosteres

Rocheblave, Luc,Bihel, Frédéric,De Michelis, Céline,Priem, Ghislaine,Courcambeek, Jér?me,Bonnet, Brice,Chermann, Jean-Claude,Kraus, Jean-Louis

, p. 3321 - 3324 (2007/10/03)

Starting from the chemical structure of the recent FDA-approved anti-HIV drug Amprenavir (Agenerase), a potent HIV-protease inhibitor, we have designed new series of Amprenavir bioisoteres in which the methylene group of the benzyl group was replaced by a

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