Cas 179532-66-2,(3aR,6S,6aS)-1,3-Bis-(3-acetyl-benzyl)-6-(5-hydroxy-pentyl)-tetrahydro-thieno[3,4-d]imidazol-2-one

179532-66-2

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Basic information

Product Name: (3aR,6S,6aS)-1,3-Bis-(3-acetyl-benzyl)-6-(5-hydroxy-pentyl)-tetrahydro-thieno[3,4-d]imidazol-2-one
Synonyms: (3aR,6S,6aS)-1,3-Bis-(3-acetyl-benzyl)-6-(5-hydroxy-pentyl)-tetrahydro-thieno[3,4-d]imidazol-2-one
CAS NO:179532-66-2
Molecular Formula:
Molecular Weight: 494.655
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: (3aR,6S,6aS)-1,3-Bis-(3-acetyl-benzyl)-6-(5-hydroxy-pentyl)-tetrahydro-thieno[3,4-d]imidazol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,6S,6aS)-1,3-Bis-(3-acetyl-benzyl)-6-(5-hydroxy-pentyl)-tetrahydro-thieno[3,4-d]imidazol-2-one(179532-66-2)
EPA Substance Registry System: (3aR,6S,6aS)-1,3-Bis-(3-acetyl-benzyl)-6-(5-hydroxy-pentyl)-tetrahydro-thieno[3,4-d]imidazol-2-one(179532-66-2)

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: 179532-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 179532-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,5,3 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 179532-66:
(8*1)+(7*7)+(6*9)+(5*5)+(4*3)+(3*2)+(2*6)+(1*6)=172
172 % 10 = 2
So 179532-66-2 is a valid CAS Registry Number.

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179532-66-2Relevant academic research and scientific papers

Synthesis of (+)-biotin derivatives as HIV-1 protease inhibitors

Han, Qi,Lafontaine, Jennifer,Bacheler, Lee T.,Rayner, Marlene M.,Klabe, Ronald M.,Erickson-Viitanen, Susan,Lam, Patrick Y.S.

, p. 1371 - 1374 (2007/10/03)

Several bis-N-alkylated (+)-biotin derivatives were synthesized and evaluated for activities against HIV-1 protease. The most potent inhibitor, 2D, synthesized in two steps from (+)-biotin, has K(i) of 0.50 μM and antiviral IC90 of 7 μM. The (+

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