53312-77-9

Usage

Uses

Used in Pharmaceutical Industry:
2-Amino-3-chlorobenzonitrile is used as an intermediate for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Amino-3-chlorobenzonitrile serves as an intermediate in the production of various agrochemicals. Its properties make it suitable for use in the synthesis of compounds that can help protect crops and enhance agricultural productivity.
Used in Dye Industry:
2-Amino-3-chlorobenzonitrile is also employed in the dye industry as an intermediate for the synthesis of different types of dyes. Its chemical properties contribute to the creation of vibrant and long-lasting colorants used in various applications.
Used in Organic Synthesis:
2-Amino-3-chlorobenzonitrile is utilized in the synthesis of various other organic compounds. Its versatility as a chemical intermediate makes it a valuable component in the development of new organic materials and compounds for various industries.
It is crucial to handle 2-Amino-3-chlorobenzonitrile with care and follow proper safety precautions when working with it due to its potential irritant properties and harmful effects if ingested.

InChI:InChI=1/C7H5ClN2/c8-6-3-1-2-5(4-9)7(6)10/h1-3H,10H2

Upstream product

• 544-92-3 copper(I) cyanide 
• 608-31-1 2,6-Dichloroaniline 

Downstream Products

• 402842-43-7 3-chloro-2-(5-oxo-5,6-dihydro-2H-thiopyran-3-ylamino)-benzonitrile 
• 397322-82-6 2-amino-3-chlorophenylformaldehyde 
• 62484-22-4 8-chloro-2,4-dioxo-1,2,3,4-tetrahydroquinazoline 
• 5621-66-9 [2-amino-3-chlorophenyl]phenylmethanone 
• 56762-32-4 1-(2-amino-3-chlorophenyl)ethan-1-one 
• 857594-97-9 2-chloro-6-(prop-1-en-2-yl)aniline 
• 19407-55-7 8-Chloro-2-phenylquinazolin-4(3H)-one 

Relevant academic research and scientific papers

A kind of 3,4-dichloro-thiazole derivatives and process for their preparation and use

The invention provides 3,4-dichloro isothiazole derivatives, their preparation method and application. The invention relates to a heterocyclic compound containing 3,4-dichloro isothiazol, and the compound is represented by the following chemical structural general formula. The invention discloses the structural general formula of the compound, a synthetic method of the compound and applications of the compound as pesticide, bactericide, anti-plant virus agent, and plant activator, and a technology of mixing the compound with agriculturally acceptable auxiliary agents or synergists for preparing pesticide, bactericide, anti-plant virus agent, and plant activator. The invention further discloses the combined application of the compound and the commercial pesticide, bactericide, anti-plant virus agent, and plant activator in controlling diseases, insect pests, and virus diseases in agriculture, forestry and gardening, and a preparation method of the compound and the commercial pesticide, bactericide, anti-plant virus agent, and plant activator.

The novel reaction of ketones with o-oxazoline-substituted anilines

A variety of ketones react with o-oxazoline-substituted anilines in the presence of catalytic amount of p-toluenesulfonic acid in dry n-butanol to form 4-amino-substituted quinolines or 4-quinolones in fair to good yields.

Evidence for Homo-Conjugation between Two Revolving 14π-Electron Systems in 10b-Methyl-10c-[2-(10b,10c-dimethyl-10b,10c-dihydropyrenyl)]-10b, 10c-dihydropyrene

Ring contraction followed by an elimination reaction on anti-9-methyl-18-trans-2-(10b,10c-dimethyl-10b,10c-dihydropyrenyl)-2,11-dithia[3,3]metacyclophane gave the desired compound 10b-methyl-10c-[2-(10b,10c-dimethyl-10b,10c-dihydropyrenyl)]-10b,10c-dihydropyrene. 1H NMR spectroscopic analysis indicated a ring current effect over a considerable distance from the macro-molecular plane of each of the aromatic rings with the two π systems freely rotating. Bathochromic shifts and peak broadening in its electronic spectrum clearly supports the presence of through-space π?π interactions between the two aromatic rings. This should serve as a good model to verify homo-conjugation effect in such a novel system where the two π systems are freely revolving. Copyright