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1-[2-(4-fluorophenyl)ethyl]-1,2,3,6-tetrahydropyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1351938-82-3 Structure
  • Basic information

    1. Product Name: 1-[2-(4-fluorophenyl)ethyl]-1,2,3,6-tetrahydropyridine
    2. Synonyms: 1-[2-(4-fluorophenyl)ethyl]-1,2,3,6-tetrahydropyridine
    3. CAS NO:1351938-82-3
    4. Molecular Formula:
    5. Molecular Weight: 205.275
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1351938-82-3.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-[2-(4-fluorophenyl)ethyl]-1,2,3,6-tetrahydropyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[2-(4-fluorophenyl)ethyl]-1,2,3,6-tetrahydropyridine(1351938-82-3)
    11. EPA Substance Registry System: 1-[2-(4-fluorophenyl)ethyl]-1,2,3,6-tetrahydropyridine(1351938-82-3)
  • 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: 1351938-82-3(Hazardous Substances Data)

1351938-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1351938-82-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,1,9,3 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1351938-82:
(9*1)+(8*3)+(7*5)+(6*1)+(5*9)+(4*3)+(3*8)+(2*8)+(1*2)=173
173 % 10 = 3
So 1351938-82-3 is a valid CAS Registry Number.

1351938-82-3Relevant articles and documents

Time-dependent slowly-reversible inhibition of monoamine oxidase A by N-substituted 1,2,3,6-tetrahydropyridines

Wichitnithad, Wisut,O'Callaghan, James P.,Miller, Diane B.,Train, Brian C.,Callery, Patrick S.

, p. 7482 - 7492 (2012/02/02)

A novel class of N-substituted tetrahydropyridine derivatives was found to have multiple kinetic mechanisms of monoamine oxidase A inhibition. Eleven structurally similar tetrahydropyridine derivatives were synthesized and evaluated as inhibitors of MAO-A and MAO-B. The most potent MAO-A inhibitor in the series, 2,4-dichlorophenoxypropyl analog 12, displayed time-dependent mixed noncompetitive inhibition. The inhibition was reversed by dialysis, indicating reversible enzyme inhibition. Evidence that the slow-binding inhibition of MAO-A with 12 involves a covalent bond was gained from stabilizing a covalent reversible intermediate product by reduction with sodium borohydride. The reduced enzyme complex was not reversible by dialysis. The results are consistent with slowly reversible, mechanism-based inhibition. Two tetrahydropyridine analogs that selectively inhibited MAO-A were characterized by kinetic mechanisms differing from the kinetic mechanism of 12. As reversible inhibitors of MAO-A, tetrahydropyridine analogs are at low risk of having an adverse effect of tyramine-induced hypertension.

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