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383909-10-2

tributyl[2-(2-phenylethynyl)phenyl]stannane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 383909-10-2 Structure

  • Basic information

    1. Product Name: tributyl[2-(2-phenylethynyl)phenyl]stannane
    2. Synonyms: tributyl[2-(2-phenylethynyl)phenyl]stannane
    3. CAS NO:383909-10-2
    4. Molecular Formula:
    5. Molecular Weight: 467.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 383909-10-2.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: tributyl[2-(2-phenylethynyl)phenyl]stannane(CAS DataBase Reference)
    10. NIST Chemistry Reference: tributyl[2-(2-phenylethynyl)phenyl]stannane(383909-10-2)
    11. EPA Substance Registry System: tributyl[2-(2-phenylethynyl)phenyl]stannane(383909-10-2)

  • 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: 383909-10-2(Hazardous Substances Data)

383909-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 383909-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,9,0 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 383909-10:
(8*3)+(7*8)+(6*3)+(5*9)+(4*0)+(3*9)+(2*1)+(1*0)=172
172 % 10 = 2
So 383909-10-2 is a valid CAS Registry Number.

383909-10-2Relevant articles and documents

A Drastic Effect of TEMPO in Zinc-Catalyzed Stannylation of Terminal Alkynes with Hydrostannanes via Dehydrogenation and Oxidative Dehydrogenation

Kai, Yuichi,Oku, Shinya,Sakurai, Kyoko,Tani, Tomohiro,Tsuchimoto, Teruhisa

, (2019/08/21)

With a system consisting of a catalytic zinc Lewis acid, pyridine, and TEMPO in a nitrile medium, terminal alkynes coupled with HSnBu3, providing alkynylstannanes with structural diversity. The resulting alkynylstannane, without being isolated, could be directly used for Pd- and Cu-catalyzed transformations to deliver internal alkynes and more intricate tin-atom-containing molecules. Mechanistic studies indicated that TEMPOSnBu3 formed in situ from TEMPO and HSnBu3 works to stannylate the terminal alkyne in collaboration with the zinc catalyst, and that both of dehydrogenation and oxidative dehydrogenation processes are uniquely involved in a single reaction. (Figure presented.).

Palladium-iminophosphine-catalysed carbostannylation of arynes: Synthesis of ortho-substituted arylstannanes

Yoshida,Honda,Shirakawa,Hiyama

, p. 1880 - 1881 (2007/10/03)

Arynes were found to insert into a carbon-tin bond of alkynyl- and vinylstannanes in the presence of a catalytic amount of a palladium-iminophosphine complex to afford ortho-substituted arylstannanes, which were convertible into a wide variety of 1,2-disu

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