158141-35-6

Usage

Uses

Used in Pharmaceutical Industry:
(3,5-dichloropyridin-2-yl)acetonitrile is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its versatility in organic synthesis allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Agrochemical Industry:
(3,5-dichloropyridin-2-yl)acetonitrile is used as an intermediate in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Synthesis of Heterocyclic Compounds:
(3,5-dichloropyridin-2-yl)acetonitrile is used as a precursor for the synthesis of heterocyclic compounds, which are important in various chemical and pharmaceutical applications.
Used as a Reagent in Organic Reactions:
(3,5-dichloropyridin-2-yl)acetonitrile is used as a reagent in organic reactions, facilitating the formation of desired products and aiding in the advancement of organic chemistry.
Used in Synthesis of Dyes and Pigments:
(3,5-dichloropyridin-2-yl)acetonitrile is used as a starting material for the synthesis of dyes, pigments, and other specialty chemicals, contributing to the development of new colorants and materials for various industries.

Upstream product

• 16063-70-0 2,3,5-trichloropyridine 
• 830348-28-2 tert-butyl cyano(3,5-dichloro-2 pyridinyl)acetate 

Downstream Products

• 830348-02-2 N-(2-(3,5-dichloropyridin-2-yl)ethyl)-2-(trifluoromethyl)benzamide 

Relevant academic research and scientific papers

METHOD FOR PRODUCING PYRIDINE COMPOUND

PROBLEM TO BE SOLVED: To provide a method for producing industrially a pyridine compound. SOLUTION: The present invention provides a method for producing a compound represented by formula (3), by processes such as a reaction between a 2-chloropyridine compound represented by formula (1) and a Grignard reagent represented by formula (2), and a method for producing an isoindolinedione compound represented by formula (8), [where R is a hydrogen atom, a hydroxy group, a halogen atom, cyano, nitro, C1-C6 alkyl, halo (C1-C6) alkyl or the like, and X is a halogen atom]. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

MANUFACTURING METHOD OF PYRIDINE DERIVATIVE

PROBLEM TO BE SOLVED: To provide an industrial manufacturing method of a pyridine derivative. SOLUTION: There are provided a manufacturing method of a compound represented by the formula (3) by reacting a 2-chloropyridine compound represented by the formula (1) and a Grignard reagent represented by the formula (2), and a manufacturing method of an isoindoline dione compound represented by the formula (8). R represents a hydrogen atom, a hydroxyl group, a halogen atom, cyano, nitro, C1 to C6 alkyl, halo(C1 to C6) alkyl or the like and X represents a halogen atom. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

7-PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES

Compounds of Formula I: (I) in which A, A1, R1, R7a, R7b, R8 and R10 have the meanings given in the specification, are DP2 receptor inhibitors useful in the treatment of useful in the treat

N-[2-(2-Pyridinyl)ethyl]benzamide compounds and their use as fungicides

Compound of general formula (I): Process for preparing this compound. Fungicidal composition comprising a compound of general formula (I). Method for treating plants by applying a compound of general formula (I) or a composition comprising it.

Design and synthesis of 3-(2-pyridyl)pyrazolo[1,5-a]pyrimidines as potent CRF1 receptor antagonists

A series of 3-(2-pyridyl)pyrazolo[1,5-a]pyrimidines was designed and synthesized as antagonists for the corticotrophin-releasing factor-1 (CRF 1) receptor. Several compounds such as 20c (Ki=10nM) exhibited good binding affinities at the CRF1 receptor. In addition, 20c had adequate solubility in water.