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77179-37-4

4-Amino-benzoic acid 1-(1-phenyl-cyclohexyl)-piperidin-4-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77179-37-4 Structure

  • Basic information

    1. Product Name: 4-Amino-benzoic acid 1-(1-phenyl-cyclohexyl)-piperidin-4-yl ester
    2. Synonyms: 4-Amino-benzoic acid 1-(1-phenyl-cyclohexyl)-piperidin-4-yl ester
    3. CAS NO:77179-37-4
    4. Molecular Formula:
    5. Molecular Weight: 378.514
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77179-37-4.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: 4-Amino-benzoic acid 1-(1-phenyl-cyclohexyl)-piperidin-4-yl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Amino-benzoic acid 1-(1-phenyl-cyclohexyl)-piperidin-4-yl ester(77179-37-4)
    11. EPA Substance Registry System: 4-Amino-benzoic acid 1-(1-phenyl-cyclohexyl)-piperidin-4-yl ester(77179-37-4)

  • 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: 77179-37-4(Hazardous Substances Data)

77179-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77179-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,7 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77179-37:
(7*7)+(6*7)+(5*1)+(4*7)+(3*9)+(2*3)+(1*7)=164
164 % 10 = 4
So 77179-37-4 is a valid CAS Registry Number.

77179-37-4Downstream Products

77179-37-4Relevant articles and documents

New Analgesic Drugs Derived from Phencyclidine

Itzhak, Yossef,Kalir, Asher,Weissman, Ben Avi,Cohen, Sasson

, p. 496 - 499 (2007/10/02)

Several esters of 1-(1-phenylcyclohexyl)-4-piperidinol (3), 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol (10) and its propionate (11), and 1-(1-phenylcyclohexyl)-4-phenylpiperidine (13) were prepared and characterized.The new compounds, which are derived from phencyclidine, exerted analgesic activity in mice.The most potent is 10, which is twice as active as morphine.The antinociceptive activity of 10, 11, and 13 could be well correlated with their potency in the mouse vas deferens bioassay, and both were completely reversed by naloxone.

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