77532-86-6

Usage

Uses

Used in Pharmaceutical Industry:
2-CHLORO-6-FORMYLBENZONITRILE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Organic Compounds Synthesis:
2-CHLORO-6-FORMYLBENZONITRILE serves as a crucial building block in the synthesis of a range of organic compounds, enabling the creation of diverse chemical structures with potential applications in various fields.
Used in Dyes and Pigments Manufacturing:
In the manufacturing of dyes and pigments, 2-CHLORO-6-FORMYLBENZONITRILE is utilized as an intermediate to produce colorants with specific characteristics, such as color intensity and stability, for use in various industries including textiles, plastics, and printing inks.
Used in Research and Development:
2-CHLORO-6-FORMYLBENZONITRILE is employed in research and development settings to explore its chemical properties and potential applications, contributing to the advancement of scientific knowledge and the discovery of new uses for 2-CHLORO-6-FORMYLBENZONITRILE.

InChI:InChI=1/C8H4ClNO/c9-8-3-1-2-6(5-11)7(8)4-10/h1-3,5H

Upstream product

• 77532-80-0 2-chloro-6-(dibromomethyl)benzonitrile 
• 863676-23-7 2-chloro-6-(bromomethyl)benzonitrile 
• 6575-09-3 2-chloro-6-methyl-benzonitrile 

Downstream Products

• 1049693-85-7 2-chloro-6-(2,2-dibromovinyl)benzonitrile 

Relevant academic research and scientific papers

CYCLIC IMIDATE LIGANDS

The present invention relates to a use of a cyclic imidate as a ligand for catalysis in which the ligand contains sub-structure (Y) as a minimal structural motive, wherein the carbon atoms and the nitrogen atom can be optionally substituted by a chemical substituent.

Efficient one-step synthesis of chiral bidentate oxazoline-alcohol ligands via a cyclic imidate ester rearrangement

Various chiral bidentate oxazoline-alcohol ligands were obtained in a straightforward one-step synthesis via a cyclic imidate ester rearrangement. These chiral ligands were tested and compared in asymmetric diethylzinc additions to aldehydes resulting in

A tandem elimination-cyclization-suzuki approach: Efficient one-pot synthesis of functionalized (Z)-3-(arylmethylene)isoindolin-1-ones

(Chemical Equation Presented) A novel and efficient one-pot regioselective elimination-cyclization-Suzuki approach was developed to afford (Z)-3-arylmethyleneisoindolin-1-ones in good to excellent yields from easily accessible o-gem-dihalovinylbenzamides and organoboron reagents.

1,3-Dihydro-3-(2-hydroxy-, 2-bromo- or 2-chloroethyl)-2H-isoindol-1-one derivatives

Derivatives of 1,3-dihydro-3-(2-hydroxyethyl) -2H-isoindol-1-one are disclosed. The derivatives are useful for treating ulcers in a mammal and for preventing or decreasing the secretion or availability of excessive amounts of gastric or hydrochloric acid in a mammal suffering from hyperchlorhydria and/or associated conditions.