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194655-89-5

(3S,5R)-3,5-Dibenzyl-pyrrolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 194655-89-5 Structure

  • Basic information

    1. Product Name: (3S,5R)-3,5-Dibenzyl-pyrrolidin-2-one
    2. Synonyms: (3S,5R)-3,5-Dibenzyl-pyrrolidin-2-one
    3. CAS NO:194655-89-5
    4. Molecular Formula:
    5. Molecular Weight: 265.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 194655-89-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3S,5R)-3,5-Dibenzyl-pyrrolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,5R)-3,5-Dibenzyl-pyrrolidin-2-one(194655-89-5)
    11. EPA Substance Registry System: (3S,5R)-3,5-Dibenzyl-pyrrolidin-2-one(194655-89-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 194655-89-5(Hazardous Substances Data)

194655-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194655-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,6,5 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 194655-89:
(8*1)+(7*9)+(6*4)+(5*6)+(4*5)+(3*5)+(2*8)+(1*9)=185
185 % 10 = 5
So 194655-89-5 is a valid CAS Registry Number.

194655-89-5Relevant articles and documents

Optimization of pyrrolidinone based HIV protease inhibitors

Sherrill, Ronald G.,Andrews, C. Webster,Bock, William J.,Davis-Ward, Ronda G.,Furfine, Eric S.,Hazen, Richard J.,Rutkowske, Randy D.,Spaltenstein, Andrew,Wright, Lois L.

, p. 81 - 84 (2007/10/03)

The synthesis and enhanced antiviral activity of a series of P1′-optimized 3,5-dibenzyl pyrrolidinone based HIV protease inhibitors is described. Optimization of P1-substituted pyrrolidinone based HIV protease inhibitors has yielded analogs with very pote

Design and synthesis of novel conformationally restricted HIV protease inhibitors

Salituro, Francesco G.,Baker, Christopher T.,Court, John J.,Deininger, David D.,Kim, Eunice E.,Li, Biquin,Novak, Perry M.,Rao, Bhisetti G.,Pazhanisamy,Porter, Margaret D.,Schairer, Wayne C.,Tung, Roger D.

, p. 3637 - 3642 (2007/10/03)

A set of HIV protease inhibitors represented by compound 2 has previously been described. Structural and conformational analysis of this compound suggested that conformational restriction of the P1/P2 portion of the molecule could lead to a novel set of potent protease inhibitors. Thus, probe compounds 3-7 were designed, synthesized, and found to be potent inhibitors of HIV protease.

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