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Methyl 2-(piperidin-3-yl)acetate hydrochloride, also known as Methyl 3-Piperidylacetate, is a chemical compound that serves as an analog of Methylphenidate, a central nervous system stimulant. It is characterized by its piperidine ring and acetate group, which contribute to its unique chemical properties and potential applications.

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  • 247259-31-0 Structure
  • Basic information

    1. Product Name: Methyl 2-(piperidin-3-yl)acetate hydrochloride
    2. Synonyms: 3-Piperidine acetate methyl ester hydrochloride;Methyl 2-(piperidin-3-yl)acetate hydrochloride;Methyl 3-Piperidylacetate Hydrochloride;3-Piperidineacetic Acid Methyl Ester Hydrochloride;methyl 2-(piperidin-3-yl)acetate;METHYL 2-(PIPERIDIN-3-YL)ACETATE HCL;Methyl 3-piperidineacetate HCl
    3. CAS NO:247259-31-0
    4. Molecular Formula: C8H15NO2.ClH
    5. Molecular Weight: 193.672
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 247259-31-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 2-(piperidin-3-yl)acetate hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-(piperidin-3-yl)acetate hydrochloride(247259-31-0)
    11. EPA Substance Registry System: Methyl 2-(piperidin-3-yl)acetate hydrochloride(247259-31-0)
  • 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: 247259-31-0(Hazardous Substances Data)

247259-31-0 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2-(piperidin-3-yl)acetate hydrochloride is used as a research chemical for the development of new drugs and therapies. Its structural similarity to Methylphenidate, a known CNS stimulant, makes it a valuable compound for studying the effects of stimulants on the central nervous system and potentially developing new treatments for conditions such as attention deficit hyperactivity disorder (ADHD) and narcolepsy.
Used in Research and Development:
Methyl 2-(piperidin-3-yl)acetate hydrochloride is used as a research tool in the field of medicinal chemistry and neuroscience. Its unique structure allows scientists to investigate the mechanisms of action of CNS stimulants and explore the potential for developing new drugs with improved efficacy and reduced side effects.
Used in Drug Synthesis:
Methyl 2-(piperidin-3-yl)acetate hydrochloride can be used as an intermediate in the synthesis of other pharmaceutical compounds. Its functional groups and structural features make it a versatile building block for the development of new drugs with potential applications in various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 247259-31-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,2,5 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 247259-31:
(8*2)+(7*4)+(6*7)+(5*2)+(4*5)+(3*9)+(2*3)+(1*1)=150
150 % 10 = 0
So 247259-31-0 is a valid CAS Registry Number.
InChI:InChI=1S/C8H15NO2.ClH/c1-11-8(10)5-7-3-2-4-9-6-7;/h7,9H,2-6H2,1H3;1H

247259-31-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-piperidin-3-ylacetate,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-Piperidine acetate methyl ester hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:247259-31-0 SDS

247259-31-0Relevant articles and documents

Synthesis and Pharmacology of Site-Specific Cocaine Abuse Treatment Agents: The Role of the Phenyl Group in Highly Modified Methylphenidate analogs as Dopamine Uptake Inhibitors

Deutsch, Howard M.,Dunn, Travis,Ye, Xiaocong,Schweri, Margaret M.

, p. 213 - 222 (2007/10/03)

A series of modified methylphenidate derivatives was synthesized and tested for inhibitory potency in [3H]WIN 35,428 binding and [3H]dopamine uptake assays using rat striatal tissue. In these compounds the role of the phenyl ring was investigated by its r

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