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CAS

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135273-60-8

Silane, dichloroethyl(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135273-60-8 Structure

  • Basic information

    1. Product Name: Silane, dichloroethyl(4-methylphenyl)-
    2. Synonyms:
    3. CAS NO:135273-60-8
    4. Molecular Formula: C9H12Cl2Si
    5. Molecular Weight: 219.186
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135273-60-8.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, dichloroethyl(4-methylphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, dichloroethyl(4-methylphenyl)-(135273-60-8)
    11. EPA Substance Registry System: Silane, dichloroethyl(4-methylphenyl)-(135273-60-8)

  • 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: 135273-60-8(Hazardous Substances Data)

135273-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135273-60-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,7 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 135273-60:
(8*1)+(7*3)+(6*5)+(5*2)+(4*7)+(3*3)+(2*6)+(1*0)=118
118 % 10 = 8
So 135273-60-8 is a valid CAS Registry Number.

135273-60-8Relevant articles and documents

Solid phase cross-coupling reaction of aryl(halo)silanes with 4-iodobenzoic acid

Homsi, Fadi,Hosoi, Kazushi,Nozaki, Kyoko,Hiyama, Tamejiro

, p. 208 - 216 (2007/10/03)

Aryl(alkyl)(halo)silanes undergo facile and efficient palladium catalyzed cross-coupling reaction with iodobenzoic acid tethered to the Wang resin. Acid cleavage releases unsymmetrical biaryl carboxylic acids with high conversions, purities and yields.

CARBONYLATIVE COUPLING REACTION OF ORGANOFLUOROSILANES WITH ORGANIC HALIDES PROMOTED BY FLUORIDE ION AND PALLADIUM CATALYST

Hatanaka, Yasuo,Fukushima, Satoshi,Hiyama, Tamejiro

, p. 2113 - 2126 (2007/10/02)

Palladium-catalyzed carbonylative cross coupling reaction of organofluorosilanes with organic halides was achieved in the presence of fluoride ion and an atmospheric pressure of carbon monoxide.Alkenyl- or arylfluorosilanes effectively underwent this reaction with alkenyl or aryl iodides in moderate to good yields.Thus, highly functionalized ketones are readily available without protection of reactive functional group such as aldehyde, ketone, ester, nitril, and alcohol.For smooth ketone formation, use of organofluorosilanes is essential; tetraorganosilanes like aryl(trimethyl)silanes, upon reaction with aryl iodides, gave aroyl fluorides instead. Key Words: carbonylative coupling; organofluorosilanes; ketone synthesis

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