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2-Pyrrolidinecarboxamide,4-fluoro-5-oxo-,(2R,4R)-rel-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 261623-77-2 Structure
  • Basic information

    1. Product Name: 2-Pyrrolidinecarboxamide,4-fluoro-5-oxo-,(2R,4R)-rel-(9CI)
    2. Synonyms: 2-Pyrrolidinecarboxamide,4-fluoro-5-oxo-,(2R,4R)-rel-(9CI)
    3. CAS NO:261623-77-2
    4. Molecular Formula: C5H7FN2O2
    5. Molecular Weight: 146.1196832
    6. EINECS: N/A
    7. Product Categories: AMIDE;HALIDE
    8. Mol File: 261623-77-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Pyrrolidinecarboxamide,4-fluoro-5-oxo-,(2R,4R)-rel-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pyrrolidinecarboxamide,4-fluoro-5-oxo-,(2R,4R)-rel-(9CI)(261623-77-2)
    11. EPA Substance Registry System: 2-Pyrrolidinecarboxamide,4-fluoro-5-oxo-,(2R,4R)-rel-(9CI)(261623-77-2)
  • 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: 261623-77-2(Hazardous Substances Data)

261623-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261623-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,6,2 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 261623-77:
(8*2)+(7*6)+(6*1)+(5*6)+(4*2)+(3*3)+(2*7)+(1*7)=132
132 % 10 = 2
So 261623-77-2 is a valid CAS Registry Number.

261623-77-2Upstream product

261623-77-2Downstream Products

261623-77-2Relevant articles and documents

Chemistry of 4-fluoroglutamic acid. Part 3. Preparation of the diastereomers of 4-fluoroglutamine and 4-fluoroisoglutamine. An enzymatic access to the antipodes of 4-amino-2-fluorobutyric acid

Tolman, Vladimír,Sedmera, Petr

, p. 5 - 10 (2007/10/03)

The pure diastereomers of 4-fluoroglutamine and 4-fluoroisoglutamine were prepared from the corresponding 4-fluoroglutamic acids. Glutamic decarboxylase treatment of the acids led to chiral 2-fluoroGABA.

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