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105584-71-2

Silane, trimethyl(phenylsulfinylmethyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105584-71-2 Structure

  • Basic information

    1. Product Name: Silane, trimethyl(phenylsulfinylmethyl)-, (E)-
    2. Synonyms:
    3. CAS NO:105584-71-2
    4. Molecular Formula: C10H14OSSi
    5. Molecular Weight: 210.372
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105584-71-2.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(phenylsulfinylmethyl)-, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, trimethyl(phenylsulfinylmethyl)-, (E)-(105584-71-2)
    11. EPA Substance Registry System: Silane, trimethyl(phenylsulfinylmethyl)-, (E)-(105584-71-2)

  • 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: 105584-71-2(Hazardous Substances Data)

105584-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105584-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,8 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105584-71:
(8*1)+(7*0)+(6*5)+(5*5)+(4*8)+(3*4)+(2*7)+(1*1)=122
122 % 10 = 2
So 105584-71-2 is a valid CAS Registry Number.

105584-71-2Downstream Products

105584-71-2Relevant articles and documents

Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides

Barbaro, Gaetano,Battaglia, Arturo,Giorgianni, Patrizia,Maccagnani, Gaetano,Macciantelli, Dante,et al.

, p. 381 - 386 (2007/10/02)

Trimethylsilyl and triphenylsilylaryl thioketones have been synthesized by acid catalysed reaction of the corresponding ketones with hydrogen sulphide.Such silylated thioketones heve been oxidized to give S-oxides and converted with diaryldiazomethanes into triaryl thiiranes; upon treatment with organolithium nucleophiles they undergo thiophilic addition.The ready desulphurization with triphenylphosphine of silylated thiirans to the corresponding silyl triaryl ethylenes is also reported.

Synthesis and Isolation of Aryl Thioaldehyde S-Oxides

Bonini, Bianca F.,Mazzanti, Germana,Zani, Paolo,Maccagnani, Gaetano,Barbaro, Gaetano,et al.

, p. 964 - 965 (2007/10/02)

(E)-Phenyl and (E)-(p-tolyl) trimethylsilyl thioketone S-oxides can be easily and stereospecifically protodesilylated into the corresponding (Z)-aryl thioaldehyde S-oxides; these stable liquid lachrimatory compounds show good reactivity as heterodienophil

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