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Silane, trimethyl[2-(1-propynyl)phenoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93782-20-8 Structure
  • Basic information

    1. Product Name: Silane, trimethyl[2-(1-propynyl)phenoxy]-
    2. Synonyms:
    3. CAS NO:93782-20-8
    4. Molecular Formula: C12H16OSi
    5. Molecular Weight: 204.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93782-20-8.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: Silane, trimethyl[2-(1-propynyl)phenoxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, trimethyl[2-(1-propynyl)phenoxy]-(93782-20-8)
    11. EPA Substance Registry System: Silane, trimethyl[2-(1-propynyl)phenoxy]-(93782-20-8)
  • 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: 93782-20-8(Hazardous Substances Data)

93782-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93782-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,8 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93782-20:
(7*9)+(6*3)+(5*7)+(4*8)+(3*2)+(2*2)+(1*0)=158
158 % 10 = 8
So 93782-20-8 is a valid CAS Registry Number.

93782-20-8Downstream Products

93782-20-8Relevant articles and documents

Gas-Phase Thermal Rearrangements of Potential Vinylidene Precursors to Silylbenzofurans and Silylbenzopyrans

Barton, Thomas J.,Groh, Brian L.

, p. 158 - 166 (1985)

In an attempt to utilize the considerable migratory aptitude of silicon in the synthesis of 3-silylbenzofurans, the flash vacuum pyrolysis (FVP) of o-phenol was found to provide not only the furan expected from vinylidene cyclization but two isomers resulting from initial 1,5-hydrogen migration from oxygen to form an intermediate allenyl ketone.FVP of 2-(trimethylsilyl)4,5-dihydrofuran produced an unprecedented gas-phase reductive elimination to a vinylidene. o-Ethynyl- and o-propynylanisoles did not afford benzopyrans through vinylidene/C-H(Me) insertion but underwent radical transformations.However, o-anisole unexpectedly extruded Me2Si to form 2-ethylbenzofuran as the only product.Various mechanisms for this remarkable decomposition are considered.The acyclic analogue 1-(trimethylsilyl)-4-methoxybut-1-yn-3-ene pyrolytically extruded not Me2Si but carbon monoxide! This is rationalized as proceeding through an initial 1,5-methyl migration from oxygen to carbon.

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