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2-(2,2-diMethoxyethyl)nicotinonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97308-52-6

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97308-52-6 Usage

Derived from nicotinic acid

2-(2,2-dimethoxyethyl)nicotinonitrile is a chemical compound that is derived from nicotinic acid, which is a water-soluble vitamin.

Two methoxyethyl groups attached to the nitrogen atom

The compound contains two methoxyethyl groups that are attached to the nitrogen atom, which gives it unique chemical properties.

Contains a nitrile group

2-(2,2-dimethoxyethyl)nicotinonitrile also contains a nitrile group (CN), which is a functional group consisting of a carbon atom triple-bonded to a nitrogen atom.

Used as a building block in the pharmaceutical industry

2-(2,2-dimethoxyethyl)nicotinonitrile is commonly used in the pharmaceutical industry as a building block for the synthesis of various biologically active compounds.

Potential as a selective enzyme inhibitor

2-(2,2-dimethoxyethyl)nicotinonitrile is known for its potential as a selective inhibitor of certain enzymes, which means it can inhibit the activity of specific enzymes in the body.

Studied for potential applications in the treatment of various diseases

Research has been conducted on 2-(2,2-dimethoxyethyl)nicotinonitrile for its potential applications in the treatment of various diseases, due to its ability to selectively inhibit certain enzymes.

Of interest for further research and development in medicinal chemistry

Due to its structural and functional properties, 2-(2,2-dimethoxyethyl)nicotinonitrile is of interest for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 97308-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,0 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 97308-52:
(7*9)+(6*7)+(5*3)+(4*0)+(3*8)+(2*5)+(1*2)=156
156 % 10 = 6
So 97308-52-6 is a valid CAS Registry Number.

97308-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,2-dimethoxyethyl)pyridine-3-carbonitrile

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:97308-52-6 SDS

97308-52-6Relevant academic research and scientific papers

HETEROARYL COMPOUNDS AND METHODS OF USE THEREOF

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Page/Page column 45, (2012/07/27)

Provided herein are heteroaryl compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. In one embodiment, the compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, such as CNS disorders and metabolic disorders, including, but not limited to, e.g., neurological disorders, psychosis, schizophrenia, obesity, and diabetes.

ANTI-VIRAL COMPOUNDS

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Page/Page column 80, (2008/12/08)

Compounds effective in inhibiting replication of Hepatitis C virus ( HCV ) or other viruses are disclosed. This invention is also directed to compositions comprising such compounds, coformulation or co-administration of such compounds with other anti-viral or therapeutic agents, processes and intermediates for the syntheses of such compounds, and methods of using such compounds for the treatment of HCV or other viral infections.

Condensed Heteroaromatic Ring Systems. III. Synthesis of Naphthyridine Derivatives by Cyclization of Ethynylpyridinecarboxamides

Sakamoto, Takao,Kondo, Yoshinori,Yamanaka, Hiroshi

, p. 626 - 633 (2007/10/02)

Four kinds of naphthyridinones, i.e. 1,6-naphthyridin-5-one, 1,7-naphthyridin-8-one, 2,6-naphthyridin-2-one, and 2,7-naphthyridin-1-one derivatives, were commonly synthesized by the intramolecular cyclization of pyridinecarboxamides having an ethynyl group or β,β-dimethoxyethyl group adjacent to the carbamoyl group.The syntheses of the starting pyridine derivatives were easily accomplished by cross-coupling of the corresponding halopyridines with acetylenes.Keywords-intramolecular cyclization; palladium catalyst; trimethylsilylacetylene; naphthyridinone; pyridineacetaldehyde; 1(2H)-isoquinolone

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