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70199-68-7

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70199-68-7 Usage

General Description

Methyl 4-pyridylacetate hydrochloride is a chemical compound with the molecular formula C8H10ClNO2. It is a derivative of the organic compound pyridine, and is a white, crystalline powder. This chemical is used in the pharmaceutical industry as a building block for the synthesis of various drugs. It is also used as an intermediate in the production of other organic compounds, and as a flavoring agent in the food and beverage industry. Methyl 4-pyridylacetate hydrochloride is a versatile compound with various industrial applications due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 70199-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,9 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70199-68:
(7*7)+(6*0)+(5*1)+(4*9)+(3*9)+(2*6)+(1*8)=137
137 % 10 = 7
So 70199-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2.ClH/c1-11-8(10)6-7-2-4-9-5-3-7;/h2-5H,6H2,1H3;1H

70199-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-pyridin-4-ylacetate,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-PYRIDINEACETIC ACID 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:70199-68-7 SDS

70199-68-7Relevant 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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