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247259-33-2

4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 247259-33-2 Structure

  • Basic information

    1. Product Name: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester
    2. Synonyms: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester;methyl (1-benzylpiperidin-4-yl)acetate;2-[1-(benzyl)-4-piperidyl]acetic acid methyl ester;2-[1-(phenylmethyl)-4-piperidinyl]acetic acid methyl ester;methyl (1-benzylpiperidin-4-yl)acetate hydrochloride;methyl 2-[1-(phenylmethyl)-4-piperidyl]acetate;methyl 2-[1-(phenylmethyl)piperidin-4-yl]acetate;methyl 2-[1-(phenylmethyl)piperidin-4-yl]ethanoate
    3. CAS NO:247259-33-2
    4. Molecular Formula: C15H21NO2
    5. Molecular Weight: 247.33274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 247259-33-2.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester(247259-33-2)
    11. EPA Substance Registry System: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester(247259-33-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 247259-33-2(Hazardous Substances Data)

247259-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 247259-33-2 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 247259-33:
(8*2)+(7*4)+(6*7)+(5*2)+(4*5)+(3*9)+(2*3)+(1*3)=152
152 % 10 = 2
So 247259-33-2 is a valid CAS Registry Number.

247259-33-2SDS

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 (1-benzylpiperidin-4-yl)acetate

1.2 Other means of identification

Product number -
Other names -

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:247259-33-2 SDS

247259-33-2Relevant articles and documents

TETRAHYDROIMDIDAZOPYRAZINE DERIVATIVES AS CGRP RECEPTOR ANTAGONISTS

-

, (2014/05/07)

The disclosure generally relates to the novel compounds of formula I, including pharmaceutically acceptable salts, which are CGRP receptor antagonists. The disclosure also relates to pharmaceutical compositions and methods for using the compounds in the t

Novel therapeutic agents for the treatment of migraine

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Page/Page column 47, (2010/02/14)

The present invention relates to compounds of Formula (I) as antagonists of calcitonin gene-related peptide receptors (“CGRP-receptor”), pharmaceutical compositions comprising them, methods for identifying them, methods of treatment using them and their u

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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