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1393462-94-6

2-(4-methylbenzoyl)-N-phenyloxirane-2-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393462-94-6 Structure

  • Basic information

    1. Product Name: 2-(4-methylbenzoyl)-N-phenyloxirane-2-carboxamide
    2. Synonyms:
    3. CAS NO:1393462-94-6
    4. Molecular Formula:
    5. Molecular Weight: 281.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393462-94-6.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: 2-(4-methylbenzoyl)-N-phenyloxirane-2-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-methylbenzoyl)-N-phenyloxirane-2-carboxamide(1393462-94-6)
    11. EPA Substance Registry System: 2-(4-methylbenzoyl)-N-phenyloxirane-2-carboxamide(1393462-94-6)

  • 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: 1393462-94-6(Hazardous Substances Data)

1393462-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393462-94-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,4,6 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1393462-94:
(9*1)+(8*3)+(7*9)+(6*3)+(5*4)+(4*6)+(3*2)+(2*9)+(1*4)=186
186 % 10 = 6
So 1393462-94-6 is a valid CAS Registry Number.

1393462-94-6Downstream Products

1393462-94-6Relevant articles and documents

Highly enantioselective epoxidation catalyzed by cinchona thioureas: Synthesis of functionalized terminal epoxides bearing a quaternary stereogenic center

Russo, Alessio,Galdi, Gerardina,Croce, Gianluca,Lattanzi, Alessandra

, p. 6152 - 6157 (2012/06/30)

A brilliant debut! Cinchona thioureas have been reported for the first time as catalysts in the area of asymmetric oxidations. They efficiently promote an unprecedented highly enantioselective epoxidation of deactivated 1,1-disubstituted alkenes to terminal epoxides containing a quaternary stereogenic center (see scheme). Copyright

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