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145065-94-7

3-Ethyl-5-oxo-2-phenyl-pyrrolidine-1-sulfonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145065-94-7 Structure

  • Basic information

    1. Product Name: 3-Ethyl-5-oxo-2-phenyl-pyrrolidine-1-sulfonyl chloride
    2. Synonyms:
    3. CAS NO:145065-94-7
    4. Molecular Formula:
    5. Molecular Weight: 287.767
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145065-94-7.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-Ethyl-5-oxo-2-phenyl-pyrrolidine-1-sulfonyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Ethyl-5-oxo-2-phenyl-pyrrolidine-1-sulfonyl chloride(145065-94-7)
    11. EPA Substance Registry System: 3-Ethyl-5-oxo-2-phenyl-pyrrolidine-1-sulfonyl chloride(145065-94-7)

  • 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: 145065-94-7(Hazardous Substances Data)

145065-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145065-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,6 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 145065-94:
(8*1)+(7*4)+(6*5)+(5*0)+(4*6)+(3*5)+(2*9)+(1*4)=127
127 % 10 = 7
So 145065-94-7 is a valid CAS Registry Number.

145065-94-7Downstream Products

145065-94-7Relevant articles and documents

A short synthesis of γ-lactams via the spontaneous ring expansion of β-lactams

Black,Olson,Abt

, p. 2729 - 2733 (1992)

β-Lactams, derived via the cycloaddition of chlorosulfonyl isocyanate to alkenes, undergo thermal rearrangement at room temperature to affort γ-lactams.

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