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CAS

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92324-30-6

1-(1-p-toluenesulfonylpiperidin-4-yl)ethan-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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  • 92324-30-6 Structure

  • Basic information

    1. Product Name: 1-(1-p-toluenesulfonylpiperidin-4-yl)ethan-1-ol
    2. Synonyms: 1-(1-p-toluenesulfonylpiperidin-4-yl)ethan-1-ol
    3. CAS NO:92324-30-6
    4. Molecular Formula:
    5. Molecular Weight: 283.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92324-30-6.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: 1-(1-p-toluenesulfonylpiperidin-4-yl)ethan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(1-p-toluenesulfonylpiperidin-4-yl)ethan-1-ol(92324-30-6)
    11. EPA Substance Registry System: 1-(1-p-toluenesulfonylpiperidin-4-yl)ethan-1-ol(92324-30-6)

  • 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: 92324-30-6(Hazardous Substances Data)

92324-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92324-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,2 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92324-30:
(7*9)+(6*2)+(5*3)+(4*2)+(3*4)+(2*3)+(1*0)=116
116 % 10 = 6
So 92324-30-6 is a valid CAS Registry Number.

92324-30-6Downstream Products

92324-30-6Relevant articles and documents

Radical Deuteration with D2O: Catalysis and Mechanistic Insights

Soulard, Valentin,Villa, Giorgio,Vollmar, Denis Patrick,Renaud, Philippe

, p. 155 - 158 (2018/01/17)

Selective incorporation of deuterium atoms into molecules is of high interest for labeling purposes and for optimizing properties of drug candidates. A mild and environmentally benign method for the deuteration of alkyl iodides via radical pathway using D2O as source of deuterium has been developed. The reaction is initiated and mediated by triethylborane in the presence of dodecanethiol as a catalyst. This method is compatible with a wide range of functional groups and provides the monodeuterated products in good yields and with a high level of deuterium incorporation. It opens promising opportunities for the development of enantioselective radical reactions. Moreover, a revision of the mechanism of the deoxygenation reaction of xanthates using R3B and water (Wood deoxygenation) is presented.

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