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297163-75-8

Silanediol, ethyl(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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  • 297163-75-8 Structure

  • Basic information

    1. Product Name: Silanediol, ethyl(4-methylphenyl)-
    2. Synonyms:
    3. CAS NO:297163-75-8
    4. Molecular Formula: C9H14O2Si
    5. Molecular Weight: 182.294
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 297163-75-8.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: Silanediol, ethyl(4-methylphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silanediol, ethyl(4-methylphenyl)-(297163-75-8)
    11. EPA Substance Registry System: Silanediol, ethyl(4-methylphenyl)-(297163-75-8)

  • 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: 297163-75-8(Hazardous Substances Data)

297163-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 297163-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,6 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 297163-75:
(8*2)+(7*9)+(6*7)+(5*1)+(4*6)+(3*3)+(2*7)+(1*5)=178
178 % 10 = 8
So 297163-75-8 is a valid CAS Registry Number.

297163-75-8Relevant articles and documents

Palladium-Catalyzed Cross-Coupling of Silanols, Silanediols, and Silanetriols Promoted by Silver(I) Oxide

Hirabayashi, Kazunori,Mori, Atsunori,Kawashima, Jun,Suguro, Masahiro,Nishihara, Yasushi,Hiyama, Tamejiro

, p. 5342 - 5349 (2000)

Palladium-catalyzed cross-coupling of aryl- or alkenylsilanols, silanediols, and silanetriols with a variety of iodoarenes by the catalysis of palladium(0) and in the presence of silver(I) oxide furnished the coupling products in good to excellent yields. The reactions of silanediols or silanetriols under similar conditions proceeded much faster than those of silanols to afford the corresponding coupling products in excellent yields within shorter reaction periods (5-12 h). The measurement of the X-ray diffraction (XRD) pattern of the silver residue after the reaction revealed that silver(I) oxide was converted to silver(I) iodide.

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