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56430-27-4

3,4,5-triphenyl-4-hydroxy-2-cyclohexenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56430-27-4 Structure

  • Basic information

    1. Product Name: 3,4,5-triphenyl-4-hydroxy-2-cyclohexenone
    2. Synonyms:
    3. CAS NO:56430-27-4
    4. Molecular Formula:
    5. Molecular Weight: 340.422
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56430-27-4.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: 3,4,5-triphenyl-4-hydroxy-2-cyclohexenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,5-triphenyl-4-hydroxy-2-cyclohexenone(56430-27-4)
    11. EPA Substance Registry System: 3,4,5-triphenyl-4-hydroxy-2-cyclohexenone(56430-27-4)

  • 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: 56430-27-4(Hazardous Substances Data)

56430-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56430-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,3 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56430-27:
(7*5)+(6*6)+(5*4)+(4*3)+(3*0)+(2*2)+(1*7)=114
114 % 10 = 4
So 56430-27-4 is a valid CAS Registry Number.

56430-27-4Downstream Products

56430-27-4Relevant articles and documents

Michael Additions of Benzoins versus Michael-Stetter Additions of Aldehydes

Castells, Josep,Dunach, Elisabeth,Geijo, Fernando,Lopez-Calahorra, Francisco,Prats, Margarita,et al.

, p. 2291 - 2294 (2007/10/02)

Triethylamine catalyzed Michael additions of benzoines to chalcone can prevail over the expected Michael-Stetter additions when certain thiazolium ion conjugate bases - prepared in situ from the pertinent thiazolium salts and triethylamine - are used as catalysts.

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