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CAS

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501953-30-6

1,3-Dioxolane, 2-(2-cyclobuten-1-yl)-2-[(2-iodophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501953-30-6 Structure

  • Basic information

    1. Product Name: 1,3-Dioxolane, 2-(2-cyclobuten-1-yl)-2-[(2-iodophenyl)methyl]-
    2. Synonyms:
    3. CAS NO:501953-30-6
    4. Molecular Formula: C14H15IO2
    5. Molecular Weight: 342.176
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501953-30-6.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: 1,3-Dioxolane, 2-(2-cyclobuten-1-yl)-2-[(2-iodophenyl)methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Dioxolane, 2-(2-cyclobuten-1-yl)-2-[(2-iodophenyl)methyl]-(501953-30-6)
    11. EPA Substance Registry System: 1,3-Dioxolane, 2-(2-cyclobuten-1-yl)-2-[(2-iodophenyl)methyl]-(501953-30-6)

  • 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: 501953-30-6(Hazardous Substances Data)

501953-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501953-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,9,5 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 501953-30:
(8*5)+(7*0)+(6*1)+(5*9)+(4*5)+(3*3)+(2*3)+(1*0)=126
126 % 10 = 6
So 501953-30-6 is a valid CAS Registry Number.

501953-30-6Downstream Products

501953-30-6Relevant articles and documents

Radical and palladium-catalyzed cyclizations to cyclobutenes: An entry to the BCD ring system of penitrem D

Rivkin, Alexey,Gonzalez-Lopez De Turiso, Felix,Nagashima, Tadamichi,Curran, Dennis P.

, p. 3719 - 3725 (2007/10/03)

A novel approach toward the synthesis of the BCD ring system of penitrem D is described. The strategy capitalizes on the fast cyclization rates of aryl radicals into cyclobutenes and allows access to a variety of fused tricyclic structures. Radical/polar

Samarium(II) iodide mediated radical/polar crossover reactions of cyclobutenes. An efficient approach to the BCD ring system of the penitrems.

Rivkin, Alexey,Nagashima, Tadamichi,Curran, Dennis P

, p. 419 - 422 (2007/10/03)

[reaction: see text] Radical/polar crossover reactions of derivatives of 1-(2-cyclobutenyl)-2-(2-iodoaryl)ethanones with acetone promoted by samarium diiodide and HMPA provide 1-(1-hydroxy-1-methylethyl)-2,2a,4,8b-tetrahydro-1H-cyclobuta[a]naphthalen-3-on

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