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1-Propanone, 3-(3,3-diphenyloxiranyl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90466-94-7 Structure
  • Basic information

    1. Product Name: 1-Propanone, 3-(3,3-diphenyloxiranyl)-1-phenyl-
    2. Synonyms:
    3. CAS NO:90466-94-7
    4. Molecular Formula: C23H20O2
    5. Molecular Weight: 328.411
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90466-94-7.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: 1-Propanone, 3-(3,3-diphenyloxiranyl)-1-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Propanone, 3-(3,3-diphenyloxiranyl)-1-phenyl-(90466-94-7)
    11. EPA Substance Registry System: 1-Propanone, 3-(3,3-diphenyloxiranyl)-1-phenyl-(90466-94-7)
  • 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: 90466-94-7(Hazardous Substances Data)

90466-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90466-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,6 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90466-94:
(7*9)+(6*0)+(5*4)+(4*6)+(3*6)+(2*9)+(1*4)=147
147 % 10 = 7
So 90466-94-7 is a valid CAS Registry Number.

90466-94-7Downstream Products

90466-94-7Relevant articles and documents

Intramolecular Olefin Epoxidation observed in the Air Oxidation of 1-Phenyl-1-diazopent-4-ene Derivatives

Miyashi, Tsutomu,Kamata, Masaki,Nishizawa, Yoshinori,Mukai, Toshio

, p. 147 - 148 (2007/10/02)

The simple air oxidation of 1-phenyl-1-diazopent-4-ene derivatives (2) under basic conditions (NaH) was found to involve an efficient intramolecular epoxidation to give epoxyketone (3), while the dye-sensitised photo-oxygenation reaction of (2) afforded k

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