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

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  • 141685-99-6 Structure
  • Basic information

    1. Product Name: Pyridine, 1,2,3,6-tetrahydro-1-methyl-4-[(4-methylphenyl)methyl]-
    2. Synonyms:
    3. CAS NO:141685-99-6
    4. Molecular Formula: C14H19N
    5. Molecular Weight: 201.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141685-99-6.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: Pyridine, 1,2,3,6-tetrahydro-1-methyl-4-[(4-methylphenyl)methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyridine, 1,2,3,6-tetrahydro-1-methyl-4-[(4-methylphenyl)methyl]-(141685-99-6)
    11. EPA Substance Registry System: Pyridine, 1,2,3,6-tetrahydro-1-methyl-4-[(4-methylphenyl)methyl]-(141685-99-6)
  • 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: 141685-99-6(Hazardous Substances Data)

141685-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141685-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,8 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141685-99:
(8*1)+(7*4)+(6*1)+(5*6)+(4*8)+(3*5)+(2*9)+(1*9)=146
146 % 10 = 6
So 141685-99-6 is a valid CAS Registry Number.

141685-99-6Downstream Products

141685-99-6Relevant articles and documents

Flexible N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine analogues: Synthesis and monoamine oxidase catalyzed bioactivation

Efange,Michelson,Remmel,Boudreau,Dutta,Freshler

, p. 3133 - 3138 (2007/10/02)

Eighteen analogues of N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) were synthesized and evaluated as substrates of monoamine oxidase. In general, the flexible analogues, characterized by the presence of a methylene (or ethylene) bridge between the aryl/heteroaryl and tetrahydropyridyl moieties, were better substrates of the enzyme than the conformationally restricted MPTP. It is suggested that the increased oxidative activity of these flexible analogues reflects enhanced binding due to the ability of the C-4-aryl/heteroaryl substituent to gain access to a hydrophobic pocket within the substrate binding site.

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