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96122-89-3

1-ethoxycarbonyl-4-(2-tolyl)piperidin-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 96122-89-3 Structure

  • Basic information

    1. Product Name: 1-ethoxycarbonyl-4-(2-tolyl)piperidin-4-ol
    2. Synonyms:
    3. CAS NO:96122-89-3
    4. Molecular Formula:
    5. Molecular Weight: 263.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96122-89-3.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-ethoxycarbonyl-4-(2-tolyl)piperidin-4-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-ethoxycarbonyl-4-(2-tolyl)piperidin-4-ol(96122-89-3)
    11. EPA Substance Registry System: 1-ethoxycarbonyl-4-(2-tolyl)piperidin-4-ol(96122-89-3)

  • 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: 96122-89-3(Hazardous Substances Data)

96122-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96122-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96122-89:
(7*9)+(6*6)+(5*1)+(4*2)+(3*2)+(2*8)+(1*9)=143
143 % 10 = 3
So 96122-89-3 is a valid CAS Registry Number.

96122-89-3Relevant articles and documents

Molecular-modeling based design, synthesis, and activity of substituted piperidines as γ-secretase inhibitors

Gundersen, Eric,Fan, Kristi,Haas, Kimberly,Huryn, Donna,Jacobsen, J. Steven,Kreft, Anthony,Martone, Robert,Mayer, Scott,Sonnenberg-Reines, June,Sun, Shaiu-Ching,Zhou, Hua

, p. 1891 - 1894 (2007/10/03)

Alzheimer's disease (AD) is a debilitating disease widely thought to be associated with the accumulation of beta amyloid (Aβ) in the brain. Inhibition of γ-secretase, one of the enzymes responsible for Aβ production, may be a useful strategy for the treatment of AD. Described below is a series of γ-secretase inhibitors designed from a scaffold identified by a ROCS [J. Comput. Chem. 1996, 17, 1653] search of the corporate database.

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