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4-Acetyl-2-cyanopyridine, a chemical compound with the molecular formula C8H6N2O, is a yellow solid that serves as a versatile intermediate in the synthesis of various pharmaceuticals and organic compounds. Its structure, featuring an acetyl group and a cyano group, endows it with a wide range of reactivity, making it a valuable building block for the creation of diverse organic molecules. 4-Acetyl-2-cyanopyridine is also utilized in the preparation of pyridine derivatives and is found in numerous research and industrial applications.

52689-18-6

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52689-18-6 Usage

Uses

Used in Pharmaceutical Industry:
4-Acetyl-2-cyanopyridine is used as a key intermediate for the synthesis of various pharmaceuticals, leveraging its versatile reactivity to facilitate the production of a broad spectrum of medicinal compounds.
Used in Organic Synthesis:
As a building block in organic synthesis, 4-Acetyl-2-cyanopyridine is employed for the creation of different types of organic molecules, contributing to the development of new chemical entities with potential applications in various fields.
Used in Pyridine Derivative Preparation:
4-Acetyl-2-cyanopyridine is utilized in the preparation of pyridine derivatives, which are important in the synthesis of a variety of chemical compounds, including those with biological and industrial significance.
Used in Research and Industrial Applications:
4-Acetyl-2-cyanopyridine is also found in various research and industrial applications, where its unique properties and reactivity are harnessed to advance scientific understanding and develop innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 52689-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,8 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52689-18:
(7*5)+(6*2)+(5*6)+(4*8)+(3*9)+(2*1)+(1*8)=146
146 % 10 = 6
So 52689-18-6 is a valid CAS Registry Number.

52689-18-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetylpyridine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-ACETYL-2-CYANOPYRIDINE

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:52689-18-6 SDS

52689-18-6Downstream Products

52689-18-6Relevant academic research and scientific papers

Casein kinase 1 (CK1) inhibitor for plants (by machine translation)

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Paragraph 0053; 0104; 0109-0112; 0117, (2020/02/14)

[Problem] to provide various lead compounds PHA derivatives, and/or circadian rhythm control agent having stronger CK1 inhibitor activity. [Solution] a compound represented by formula I, or a salt thereof or a solvate thereof. (R1 The, H or C1 - 5 A straight-chain, branched or cyclic alkyl group, alkenyl group or alkynyl group, R2 The, H, halogen (F, Cl, Br or I), or a C1 - 4 The alkyl group, the ring A, 5 - 8 membered lactam ring showing; however, R1 And R2 Except H together. )[Drawing] no (by machine translation)

METABOTROPIC GLUTAMATE RECEPTOR NEGATIVE ALLOSTERIC MODULATORS (NAMS) AND USES THEREOF

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, (2016/01/01)

Provided herein are small molecule active metabotropic glutamate subtype-2 and -3 receptor negative allosteric modulators (NAMs), compositions comprising the compounds, and methods of using the compounds and compositions.

Preparation of cyanopyridines by direct cyanation

Katritzky, Alan R.,Scriven, Eric F. V.,Majumder, Suman,Tu, Hongbin,Vakulenko, Anatoliy V.,Akhmedov, Novruz G.,Murugan, Ramiah

, p. 993 - 997 (2007/10/03)

After pretreatment with nitric acid and trifluoroacetic anhydride, aqueous potassium cyanide converted pyridines 1a-1 into their corresponding 2-cyano derivatives 4a-1 in an average yield of 52%. Georg Thieme Verlag Stuttgart.

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