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114760-75-7

1-Phenyl-3-methyl-cyclohexylpiperidin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114760-75-7 Structure

  • Basic information

    1. Product Name: 1-Phenyl-3-methyl-cyclohexylpiperidin
    2. Synonyms: 1-Phenyl-3-methyl-cyclohexylpiperidin
    3. CAS NO:114760-75-7
    4. Molecular Formula:
    5. Molecular Weight: 257.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114760-75-7.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-Phenyl-3-methyl-cyclohexylpiperidin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Phenyl-3-methyl-cyclohexylpiperidin(114760-75-7)
    11. EPA Substance Registry System: 1-Phenyl-3-methyl-cyclohexylpiperidin(114760-75-7)

  • 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: 114760-75-7(Hazardous Substances Data)

114760-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114760-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114760-75:
(8*1)+(7*1)+(6*4)+(5*7)+(4*6)+(3*0)+(2*7)+(1*5)=117
117 % 10 = 7
So 114760-75-7 is a valid CAS Registry Number.

114760-75-7Downstream Products

114760-75-7Relevant articles and documents

Synthesis, pharmacological action, and receptor binding affinity of the enantiomeric 1-(1-phenyl-3-methylcyclohexyl)piperidines

Thurkauf,Hillery,Mattson,Jacobsen,Rice

, p. 1625 - 1628 (2007/10/02)

The cis and trans enantiomers of the 1-(1-phenyl-3-methylcyclohexyl)piperidines were prepared from either 3(R)- or 3(S)-methylcyclohexanone through the Bruylents reaction or a modified azide route, respectively. Separation of the intermediate amines (5 an

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