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CAS 1400742-68-8

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Methyl α-(3,4-dichlorophenyl)-2-piperidineacetate

Description:
Methyl α-(3,4-dichlorophenyl)-2-piperidineacetate, identified by its CAS number 1400742-68-8, is a chemical compound that belongs to the class of piperidine derivatives. This substance features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and is substituted with a dichlorophenyl group, indicating the presence of two chlorine atoms on a phenyl ring at the 3 and 4 positions. The compound also contains an acetate functional group, which contributes to its reactivity and solubility characteristics. Typically, compounds of this nature may exhibit biological activity, making them of interest in medicinal chemistry and pharmacology. The presence of halogen substituents often influences the compound's lipophilicity and potential interactions with biological targets. As with many organic compounds, its physical properties such as melting point, boiling point, and solubility would depend on the specific molecular structure and intermolecular interactions. Safety and handling precautions are essential when working with such compounds due to potential toxicity or reactivity.
Formula:C14H17Cl2NO2
InChI:InChI=1S/C14H17Cl2NO2/c1-19-14(18)13(12-4-2-3-7-17-12)9-5-6-10(15)11(16)8-9/h5-6,8,12-13,17H,2-4,7H2,1H3
InChI key:InChIKey=JUKMAYKVHWKRKY-UHFFFAOYSA-N
SMILES:C(C(OC)=O)(C1=CC(Cl)=C(Cl)C=C1)C2CCCCN2
Synonyms:
  • Methyl α-(3,4-dichlorophenyl)-2-piperidineacetate
  • 2-Piperidineacetic acid, α-(3,4-dichlorophenyl)-, methyl ester
  • Methyl 2-(3,4-dichlorophenyl)-2-(piperidin-2-yl)acetate
  • 3,4-Dichloromethylphenidate
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Found 1 products.
  • 3,4-Dichloromethylphenidate
    Biosynth
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    3,4-Dichloromethylphenidate

    Controlled Product
    CAS:
    3,4-Dichloromethylphenidate is a synthetic cannabinoid that is structurally related to amphetamine. It has been detected in the urine of drug users and is used as a substitute for cocaine. 3,4-Dichloromethylphenidate binds to the dopamine transporter, serotonin transporter, and norepinephrine transporter proteins in the brain. The binding of 3,4-Dichloromethylphenidate to these proteins inhibits the reuptake of these neurotransmitters into the presynaptic neuron, leading to an increase in extracellular concentrations of monoamines. This leads to increased levels of dopamine in the striatum and nucleus accumbens and increased levels of serotonin in brain regions that control mood and appetite. 3,4-Dichloromethylphenidate also inhibits the activity of human liver carboxylesterase 1 (CES1). Inhibition of CES1 causes an accumulation of toxic metabolites such as phenethylam
    Formula:C14H17Cl2NO2
    Purity:Min. 95%
    Color and Shape:Yellow solid.
    Molecular weight:302.2 g/mol

    Ref: 3D-FD31747

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