355022-17-2

Usage

Uses

Used in Pharmaceutical Industry:
4-(Isopropylamino)-3-nitrobenzonitrile is used as an intermediate in the synthesis of various drugs, leveraging its chemical properties to facilitate the development of new pharmaceutical compounds. The isopropylamino group provides opportunities for interactions with other molecules, which can be crucial in the design of effective drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(Isopropylamino)-3-nitrobenzonitrile serves as a key intermediate in the production of agrochemical compounds, contributing to the development of pesticides, herbicides, and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used in Dye Industry:
4-(ISOPROPYLAMINO)-3-NITROBENZONITRILE is also utilized in the dye industry as an intermediate for the synthesis of various dyes, taking advantage of its chemical structure to create a range of colorants used in textiles, plastics, and other applications.
Used in Organic Chemistry Research:
4-(Isopropylamino)-3-nitrobenzonitrile is employed as a valuable compound in organic chemistry research, where its unique structure and functional groups are explored for potential reactions and modifications, contributing to the advancement of organic chemistry knowledge and techniques.
Used in Chemical Modification:
The presence of the nitro and cyano groups in 4-(Isopropylamino)-3-nitrobenzonitrile allows for further chemical modifications, making it a suitable candidate for the development of new compounds with tailored properties for specific applications.

InChI:InChI=1/C10H11N3O2/c1-7(2)12-9-4-3-8(6-11)5-10(9)13(14)15/h3-5,7,12H,1-2H3

Upstream product

• 1009-35-4 4-fluoro-3-nitrobenzonitrile 
• 75-31-0 isopropylamine 
• 939-80-0 4-chloro-3-nitrobenzonitrile 

Downstream Products

• 355022-36-5 4-(5-cyano-1-isopropyl-1H-benzoimidazol-2-yl)-benzoic acid 
• 475490-09-6 2-(4-fluoro-phenyl)-1-isopropyl-1H-benzoimidazole-5-carbonitrile 
• 355022-20-7 4-(isopropylamino)-3-aminobenzonitrile 

Relevant academic research and scientific papers

Oxygen-containing five-membered heterocyclic compound, synthesis method, pharmaceutical composition and application

The invention discloses an oxygen-containing five-membered heterocyclic compound, a synthesis method, a pharmaceutical composition and application thereof, and belongs to the technical field of medicines and preparation and application thereof. The oxygen-containing five-membered heterocycle has the biological activity of inhibiting the protein tyrosine phosphatase SHP2, can be used as a tool compound for researching the biological function relevance of the protein tyrosine phosphatase SHP2 in the cell signal transduction process, and provides a new means for preventing and treating cancers and metabolic and immune diseases.

Small Sequence-Sensitive Compounds for Specific Recognition of the G?C Base Pair in DNA Minor Groove

A series of small diamidines with thiophene and modified N-alkylbenzimidazole σ-hole module represent specific binding to single G?C base pair (bp) DNA sequence. The variation of N-alkyl or aromatic rings were sensitive to microstructures of the DNA minor

1-Alkyl-benzotriazole-5-carboxylic acids are highly selective agonists of the human orphan G-protein-coupled receptor GPR109b

1-Substituted benzotriazole carboxylic acids have been identified as the first reported examples of selective small-molecule agonists of the human orphan G-protein-coupled receptor GPR109b (HM74), a low-affinity receptor for the HDL-raising drug niacin. N

Synthesis of some new 2-substituted-phenyl-1H-benzimidazole-5-carbonitriles and their potent activity against Candida species

New 2-substituted-phenyl-1H-benzimidazole-5-carboxylic acids (35, 38), ethyl-5-carboxylate (36), -5-carboxamides (37, 39),-5-carboxaldehyde (42), -5-chloro (40), -5-trifluoromethyl (41), and -5-carbonitriles (44-53, 55-67), -6-carbonitrile (54) were prepa

Synthesis and antimicrobial activity of some new 2-phenyl-N-substituted carboxamido-1H-benzimidazole derivatives

Some 1H-benzimidazole-carboxamide derivatives were prepared and their antimicrobial activities against Staphyloccus aureus, Escherichia coli and Candida albicans evaluated. Compounds 18, 22, and 25 exhibited the best activity against Candida albicans.