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1441317-11-8

2-methyl-3-(triphenylsilyloxy)butan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1441317-11-8 Structure

  • Basic information

    1. Product Name: 2-methyl-3-(triphenylsilyloxy)butan-2-ol
    2. Synonyms: 2-methyl-3-(triphenylsilyloxy)butan-2-ol
    3. CAS NO:1441317-11-8
    4. Molecular Formula:
    5. Molecular Weight: 362.544
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1441317-11-8.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: 2-methyl-3-(triphenylsilyloxy)butan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl-3-(triphenylsilyloxy)butan-2-ol(1441317-11-8)
    11. EPA Substance Registry System: 2-methyl-3-(triphenylsilyloxy)butan-2-ol(1441317-11-8)

  • 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: 1441317-11-8(Hazardous Substances Data)

1441317-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1441317-11-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,1,3,1 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1441317-11:
(9*1)+(8*4)+(7*4)+(6*1)+(5*3)+(4*1)+(3*7)+(2*1)+(1*1)=118
118 % 10 = 8
So 1441317-11-8 is a valid CAS Registry Number.

1441317-11-8Downstream Products

1441317-11-8Relevant articles and documents

Chemoselective hydrosilylation of hydroxyketones

Lage, Marta L.,Bader, Scott J.,Sa-Ei, Kanicha,Montgomery, John

, p. 5609 - 5613 (2013)

A chemoselective method for the hydrosilylation of ketones has been developed, using the combination of triphenylsilane and a catalyst prepared from Ni(COD)2 and the simple N-heterocyclic carbene IMes. The most notable feature of this method is that free hydroxyls are largely unaffected, thus providing a simple one-step procedure for the conversion of hydroxyketones to mono-protected diols, wherein the protecting group is exclusively installed on the ketone-derived hydroxyl. The process is typically high yielding with both simple ketones and more complex hydroxyketone substrates.

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