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1-(4-Fluorophenyl)-5-oxopyrrolidine-3-carbohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 669696-68-8 Structure
  • Basic information

    1. Product Name: 1-(4-Fluorophenyl)-5-oxopyrrolidine-3-carbohydrazide
    2. Synonyms: 1-(4-Fluorophenyl)-5-oxopyrrolidine-3-carbohydrazide
    3. CAS NO:669696-68-8
    4. Molecular Formula: C11H12FN3O2
    5. Molecular Weight: 237.2302832
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 669696-68-8.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: 1-(4-Fluorophenyl)-5-oxopyrrolidine-3-carbohydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Fluorophenyl)-5-oxopyrrolidine-3-carbohydrazide(669696-68-8)
    11. EPA Substance Registry System: 1-(4-Fluorophenyl)-5-oxopyrrolidine-3-carbohydrazide(669696-68-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 669696-68-8(Hazardous Substances Data)

669696-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 669696-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,6,9 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 669696-68:
(8*6)+(7*6)+(6*9)+(5*6)+(4*9)+(3*6)+(2*6)+(1*8)=248
248 % 10 = 8
So 669696-68-8 is a valid CAS Registry Number.

669696-68-8Relevant articles and documents

Cyclization products of N-fluorophenyl-β-alanines and their properties

Vaickelioniene,Mickevicius

, p. 753 - 760 (2008/02/04)

Interaction of 2-and 4-fluorophenylamines with acrylic and itaconic acids leads to the synthesis of the corresponding N-substituted β-alanines, the cyclization of which leads to derivatives of dihydropyrimidinone, 4-carboxy-2-pyrrolidinone, and tetrahydro

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