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96288-20-9

1,1-dibromo-2-(1-phenylethenyl)cyclopropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 96288-20-9 Structure

  • Basic information

    1. Product Name: 1,1-dibromo-2-(1-phenylethenyl)cyclopropane
    2. Synonyms: 1,1-dibromo-2-(1-phenylethenyl)cyclopropane
    3. CAS NO:96288-20-9
    4. Molecular Formula:
    5. Molecular Weight: 302.008
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96288-20-9.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: 1,1-dibromo-2-(1-phenylethenyl)cyclopropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-dibromo-2-(1-phenylethenyl)cyclopropane(96288-20-9)
    11. EPA Substance Registry System: 1,1-dibromo-2-(1-phenylethenyl)cyclopropane(96288-20-9)

  • 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: 96288-20-9(Hazardous Substances Data)

96288-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96288-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,8 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96288-20:
(7*9)+(6*6)+(5*2)+(4*8)+(3*8)+(2*2)+(1*0)=169
169 % 10 = 9
So 96288-20-9 is a valid CAS Registry Number.

96288-20-9Relevant articles and documents

Photochemical reduction of gem-Dihalocyclopropanes. III. Debromination of some compounds containing two 1,1-dibromocyclopropane moieties

Sydnes, Leiv K.,vrebo, Hans H.,Engebretsen, Thoralf

, p. 417 - 424 (2007/10/03)

2,2,2′,2′-Tetrabromo-1-phenylbicyclopropyl and 1,1-dibromo-2-(2,2-dibromo-cyclopropyl)methyl-2-phenylcyclopropane have been synthesized, analyzed by X-ray crystallographic techniques, and exposed to acetone-sensitized irradiation. The former compound, whi

Chemistry of gem-Dihalocyclopropanes. XX. The Effect of Methyl and Phenyl Substituents on the Vinylcyclopropylidene-Cyclopentenylidene Rearrangement

Holm, Kjetil H.,Skatteboel, Lars

, p. 783 - 794 (2007/10/02)

Reactions of gem-dibromocyclopropanes of the general structure 1 with methyllithium have been studied.In the most cases cyclopentadienes and/or vinylallenes are the products formed.The results obtained give evidence of a profound substituent effect on the carbene-carbene rearrangement leading to cyclopentadienes.We believe the effect is essentially steric in origin.The results support the mechanism proposed for the rearrangement.

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