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((E)-1-Benzenesulfonyl-3-phenyl-allyl)-trimethyl-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134436-10-5 Structure
  • Basic information

    1. Product Name: ((E)-1-Benzenesulfonyl-3-phenyl-allyl)-trimethyl-silane
    2. Synonyms: ((E)-1-Benzenesulfonyl-3-phenyl-allyl)-trimethyl-silane
    3. CAS NO:134436-10-5
    4. Molecular Formula:
    5. Molecular Weight: 330.523
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134436-10-5.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: ((E)-1-Benzenesulfonyl-3-phenyl-allyl)-trimethyl-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((E)-1-Benzenesulfonyl-3-phenyl-allyl)-trimethyl-silane(134436-10-5)
    11. EPA Substance Registry System: ((E)-1-Benzenesulfonyl-3-phenyl-allyl)-trimethyl-silane(134436-10-5)
  • 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: 134436-10-5(Hazardous Substances Data)

134436-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134436-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 134436-10:
(8*1)+(7*3)+(6*4)+(5*4)+(4*3)+(3*6)+(2*1)+(1*0)=105
105 % 10 = 5
So 134436-10-5 is a valid CAS Registry Number.

134436-10-5Relevant articles and documents

Integrated chemical process. One-pot preparation of acetylenes by Peterson-sulfone elimination

Orita, Akihiro,Yoshioka, Naonori,Otera, Junzo

, p. 1023 - 1024 (1997)

Integration of silylation of α-sulfonyl carbanion, addition of the anion of the resulting α-silyl sulfone to aldehyde, Peterson elimination, and sulfone elimination leads to one-pot synthesis of acetylenes.

Integrated Chemical Process: One-Pot Double Elimination Method for Acetylenes

Orita, Akihiro,Yoshioka, Naonori,Struwe, Petra,Braier, Arnold,Beckmann, Anke,Otera, Junzo

, p. 1355 - 1363 (2007/10/03)

A novel one-pot process for synthesis of acetylenes has been achieved in which the following series of steps are integrated: addition of an α-anion of sulfone to aldehyde; trapping of the resulting adduct to incorporate a leaving group, and double elimination of this intermediate. Consolidation of Peterson elimination renders the process much simpler. This method provides a convenient and high-yielding access to a variety of enynes and polyynes as well as to functionally substituted aryl acetylenes containing halogen(s) or acetal groups, which are useful building blocks for aryl acetylene scaffolds. Iteration of the one-pot generation of acetylenic bonds provides a new metodology for the buildup of aryl acetylene skeletons.

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