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142744-09-0

trans-2-trimethylsilylcyclohexan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 142744-09-0 Structure

  • Basic information

    1. Product Name: trans-2-trimethylsilylcyclohexan-1-ol
    2. Synonyms:
    3. CAS NO:142744-09-0
    4. Molecular Formula:
    5. Molecular Weight: 172.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142744-09-0.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: trans-2-trimethylsilylcyclohexan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-2-trimethylsilylcyclohexan-1-ol(142744-09-0)
    11. EPA Substance Registry System: trans-2-trimethylsilylcyclohexan-1-ol(142744-09-0)

  • 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: 142744-09-0(Hazardous Substances Data)

142744-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142744-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,4 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142744-09:
(8*1)+(7*4)+(6*2)+(5*7)+(4*4)+(3*4)+(2*0)+(1*9)=120
120 % 10 = 0
So 142744-09-0 is a valid CAS Registry Number.

142744-09-0Relevant articles and documents

Stereoelectronic Effect of the Trimethylsilyl Substituent upon C-O Bond Lengths at the β Position: Some Structural Studies

White, Jonanthan M.,Robertson, Glen B.

, p. 4638 - 4644 (2007/10/02)

Results of low-temperature (130 K) crystal structure analyses for seven β-trimethylsilyl-substituted cyclohexylnitrobenzoate esters are reported.For those molecules (three) with the Si-C and C-O bonds antiperiplanar the C-O bond lengths are increased by 0

Some Epoxide Ring-opening Reactions of αβ-Epoxysilanes

Davis, Anthony P.,Hughes, Gwyneth J.,Lowndes, Peter R.,Robbins, Catherine M.,Thomas, Elizabeth J.,Whitham, Gordon H.

, p. 1934 - 1941 (2007/10/02)

Epoxide ring-opening of 1,2-epoxy-1-trimethylsilylcyclohexane (3) has given a range of the 2-substituted 2-trimethylsilylcyclohexanols (4; X = H, OH, OMe, OCH2CH=CH2, Br, I, SCN) in which attack by nucleophile has occured at the carbon α to silicon.The products (4) have been transformed into a number of functionalised silanes, including the silyl-episulphide (9).Other epoxides which have been less extensively studied are the conformationally biased epoxysilanes (10) and (11), the eight-membered ring epoxysilanes (17) and (21) and the two stereoisomeric 2,3-epoxy-3-trimethylsilylpentanes (26) and (29).Epoxide ring-opening adducts were obtained after treatment with H+-MeOH in all cases except for compound (17), where the bicyclic alcohol (18) was formed by a transannular reaction.

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