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106877-54-7

1,4-di(4-phenyl-4-hydantoinyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106877-54-7 Structure

  • Basic information

    1. Product Name: 1,4-di(4-phenyl-4-hydantoinyl)benzene
    2. Synonyms:
    3. CAS NO:106877-54-7
    4. Molecular Formula:
    5. Molecular Weight: 426.431
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106877-54-7.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: 1,4-di(4-phenyl-4-hydantoinyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-di(4-phenyl-4-hydantoinyl)benzene(106877-54-7)
    11. EPA Substance Registry System: 1,4-di(4-phenyl-4-hydantoinyl)benzene(106877-54-7)

  • 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: 106877-54-7(Hazardous Substances Data)

106877-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106877-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 106877-54:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*7)+(2*5)+(1*4)=147
147 % 10 = 7
So 106877-54-7 is a valid CAS Registry Number.

106877-54-7Downstream Products

106877-54-7Relevant articles and documents

REACTION OF BIS-α-DIKETONES WITH UREA IN AN ALKALINE MEDIUM

Savchenko, T. I.,Yatsimirskii, A. K.

, p. 1117 - 1122 (2007/10/02)

The condensation of bis-α-diketones C6H5COCOArCOCOC6H5 and urea with the formation of new hydantoins was investigated in an alkaline medium.The dependence of the reactivity of the bis-α-diketones on the central aryl fragment is described satisfactorily on the basis of a Hammett correlation.It was established that 1,4-di(phenyloxalyl)benzene has high sensitivity to nucleophilic attack, due to the mutal effect of the α-dicarbonyl reaction centers.From analysis of the 13C NMR and UV spectra it follows that the reactivity is probably determined not by the difference in the electron distribution at the carbons of the carbonyl groups but by their steric orientation.

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