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76669-71-1

3-Oxo-1-pyrazolidin-1-carboximidsaeure-phenylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76669-71-1 Structure

  • Basic information

    1. Product Name: 3-Oxo-1-pyrazolidin-1-carboximidsaeure-phenylester
    2. Synonyms:
    3. CAS NO:76669-71-1
    4. Molecular Formula:
    5. Molecular Weight: 281.314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76669-71-1.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: 3-Oxo-1-pyrazolidin-1-carboximidsaeure-phenylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Oxo-1-pyrazolidin-1-carboximidsaeure-phenylester(76669-71-1)
    11. EPA Substance Registry System: 3-Oxo-1-pyrazolidin-1-carboximidsaeure-phenylester(76669-71-1)

  • 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: 76669-71-1(Hazardous Substances Data)

76669-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76669-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76669-71:
(7*7)+(6*6)+(5*6)+(4*6)+(3*9)+(2*7)+(1*1)=181
181 % 10 = 1
So 76669-71-1 is a valid CAS Registry Number.

76669-71-1Relevant articles and documents

Reaction of Cyanates with 3-Pyrazolidinones

Neitzel, Michael,Zinner, Gerwalt

, p. 1907 - 1912 (2007/10/02)

Addition of 3-pyrazolidinones 1 to cyanates 2 (phenyl, 2,2,2-trichloroethyl, and trifluoroethyl cyanate) leads to the N-1-carboximidates 3 which have been transformed into the hydrochlorides 6.The IR and 1H-NMR spectra of 3 and 6 are compared with those of the N-1-carbamoyl derivates 4 and of the N-1-benzoyl derivates 5.

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