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CAS

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676127-79-0

L-Prolinamide, (2R)-2-butyl-N-(phenylmethoxy)-b-alanyl-N-(5-fluoro-2-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 676127-79-0 Structure

  • Basic information

    1. Product Name: L-Prolinamide, (2R)-2-butyl-N-(phenylmethoxy)-b-alanyl-N-(5-fluoro-2-pyridinyl)-
    2. Synonyms:
    3. CAS NO:676127-79-0
    4. Molecular Formula: C24H31FN4O3
    5. Molecular Weight: 442.534
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 676127-79-0.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: L-Prolinamide, (2R)-2-butyl-N-(phenylmethoxy)-b-alanyl-N-(5-fluoro-2-pyridinyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Prolinamide, (2R)-2-butyl-N-(phenylmethoxy)-b-alanyl-N-(5-fluoro-2-pyridinyl)-(676127-79-0)
    11. EPA Substance Registry System: L-Prolinamide, (2R)-2-butyl-N-(phenylmethoxy)-b-alanyl-N-(5-fluoro-2-pyridinyl)-(676127-79-0)

  • 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: 676127-79-0(Hazardous Substances Data)

676127-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 676127-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,1,2 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 676127-79:
(8*6)+(7*7)+(6*6)+(5*1)+(4*2)+(3*7)+(2*7)+(1*9)=190
190 % 10 = 0
So 676127-79-0 is a valid CAS Registry Number.

676127-79-0Relevant articles and documents

β-amino amides from β-lactams: Application to the formal synthesis of a peptide-deformylase inhibitor

Jiang, Xinglong,Prasad, Kapa,Prashad, Mahavir,Slade, Joel,Repi?, Oljan,Blacklock, Thomas J.

, p. 3179 - 3181 (2008/02/13)

A facile and a practical synthesis of peptide-deformylase inhibitor 1 is described using an acid-catalyzed aminolysis of β-lactam 12 with pyrrolidine 6 as the key transformation. In addition, simplified conditions for the conversion of a β-hydroxy acid to

PROCESS FOR PREPARING INTERMEDIATES

-

Page 21, (2008/06/13)

The present invention is directed to a process for preparing intermediates that are useful to prepare certain antibacterial N-formyl hydroxylamine compounds which are peptide deformylase inhibitors. The process makes use α β-lactam intermediate. Certain o

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