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CAS

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65267-08-5

Mercury, bis(2,2-diphenylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65267-08-5 Structure

  • Basic information

    1. Product Name: Mercury, bis(2,2-diphenylethenyl)-
    2. Synonyms:
    3. CAS NO:65267-08-5
    4. Molecular Formula: C28H22Hg
    5. Molecular Weight: 559.073
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65267-08-5.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: Mercury, bis(2,2-diphenylethenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Mercury, bis(2,2-diphenylethenyl)-(65267-08-5)
    11. EPA Substance Registry System: Mercury, bis(2,2-diphenylethenyl)-(65267-08-5)

  • 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: 65267-08-5(Hazardous Substances Data)

65267-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65267-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65267-08:
(7*6)+(6*5)+(5*2)+(4*6)+(3*7)+(2*0)+(1*8)=135
135 % 10 = 5
So 65267-08-5 is a valid CAS Registry Number.

65267-08-5Upstream product

65267-08-5Relevant articles and documents

The α-Vinylation of β-Dicarbonyl Compounds by Alk-1-enyl-lead Triacetates

Moloney, Mark G.,Pinhey, John T.

, p. 2847 - 2854 (2007/10/02)

Treatment of (E,E)-distyrylmercury (1) with lead tetra-acetate gave a mixture of (E)-styrylmercury acetate (3) and (E)-styryl-lead triacetate (2), which decomposed to (E)-styryl acetate (4) and lead(II) acetate.The vinyl-lead compound (2), generated in this way, reacted rapidly with β-keto ester (5) to give the α-(E)-styryl derivative (6) in synthetically useful yield.This procedure for the α-vinylation of (5) has been applied to the divinylmercury compounds (7)-(13), and to the synthesis of the α-(E)-styryl β-dicarbonyl compounds (28), (30), (32), and (34).Compounds (6), (28), (30), (32), and (34).Compounds (6), (28), (30), (32), and (34) have also been produced by reaction with lead compound (2) generated by reaction of tributyl-(E)-styrylstannane (36) and lead tetra-acetate.Isolation of the relatively stable cyclopent-1-enyl-lead triacetate (21b), and its reaction with keto ester (5) to give a quantitative yield of compound (18), provided evidence that vinyl-lead triacetates are the vinylating species.

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