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CAS

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867375-24-4

[(3-decyn-2-oxy)dimesitylsilyl]trimethylstannane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 867375-24-4 Structure

  • Basic information

    1. Product Name: [(3-decyn-2-oxy)dimesitylsilyl]trimethylstannane
    2. Synonyms: [(3-decyn-2-oxy)dimesitylsilyl]trimethylstannane
    3. CAS NO:867375-24-4
    4. Molecular Formula:
    5. Molecular Weight: 583.517
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 867375-24-4.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: [(3-decyn-2-oxy)dimesitylsilyl]trimethylstannane(CAS DataBase Reference)
    10. NIST Chemistry Reference: [(3-decyn-2-oxy)dimesitylsilyl]trimethylstannane(867375-24-4)
    11. EPA Substance Registry System: [(3-decyn-2-oxy)dimesitylsilyl]trimethylstannane(867375-24-4)

  • 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: 867375-24-4(Hazardous Substances Data)

867375-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 867375-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,3,7 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 867375-24:
(8*8)+(7*6)+(6*7)+(5*3)+(4*7)+(3*5)+(2*2)+(1*4)=214
214 % 10 = 4
So 867375-24-4 is a valid CAS Registry Number.

867375-24-4Downstream Products

867375-24-4Relevant articles and documents

Substituent-control of two modes of intramolecular reactions of allyloxy-silyllithiums and propargyloxy-silyllithiums

Kawachi, Atsushi,Maeda, Hirofumi,Tamao, Kohei

, p. 1520 - 1527 (2007/10/03)

Intramolecular reactions of the [(allyloxy)silyl]lithiums and the [(propargyloxy)silyl]lithiums have been investigated. The [(allyloxy)silyl] lithiums proceed in two reaction modes depending on the electronic effect of the substituents at the terminus of the olefin. The [(allyloxy)silyl]lithiums bearing hydrogen, n-C6H13, or trimethylsilyl substituent undergo the [2,3]-sila-Wittig rearrangement to afford the lithium allylsilanolates, while those bearing the phenyl, thienyl, or triphenylsilyl substituent experience the 4-exo-trig cyclization and subsequent 1,3-cycloelimination to give the lithium cyclopropylsilanolates. On the other hand, the [(propargyloxy)silyl]lithiums preferentially undergo the 4-exo-dig cyclization over the [2,3]-sila-Wittig rearrangement in all cases.

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