Cas 149976-33-0,[(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

149976-33-0

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Basic information

Product Name: [(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester
Synonyms: [(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester
CAS NO:149976-33-0
Molecular Formula:
Molecular Weight: 607.866
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,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester(149976-33-0)
EPA Substance Registry System: [(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester(149976-33-0)

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: 149976-33-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149976-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,9,7 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 149976-33:
(8*1)+(7*4)+(6*9)+(5*9)+(4*7)+(3*6)+(2*3)+(1*3)=190
190 % 10 = 0
So 149976-33-0 is a valid CAS Registry Number.

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149976-33-0Relevant academic research and scientific papers

Rational design, synthesis, and crystallographic analysis of a hydroxyethylene-based HIV-1 protease inhibitor containing a heterocyclic P1'-P2' amide bond isostere

Thompson,Murthy,Zhao,Winborne,Green,Fisher,DesJarlais,Tomaszek Jr.,Meek,Gleason,Abdel-Meguid

, p. 3100 - 3107 (2007/10/02)

The rational design and synthesis of a highly potent inhibitor of HIV-1 protease have been accomplished. The inhibitor, SB 206343, is based on a model derived from the structure of the MVT-101/HIV-1 protease complex and contains a 4(5)-acylimidazole ring

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