115753-34-9

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

It is derived from benzenedicarbonitrile, which is a compound consisting of a benzene ring with two cyano groups (CN) attached to it.

Explanation

This name provides more information about the specific functional groups present in the compound, such as the amino (NH2) and bromo (Br) groups.

Explanation

The compound is used as a building block or reagent in the synthesis of various pharmaceuticals, dyes, and other organic compounds due to its versatile chemical structure.

Explanation

The compound is a solid, appearing as a white to off-white powder when in its pure form.

Explanation

The compound does not dissolve well in water but can dissolve in certain organic solvents, which is important for its use in chemical reactions and synthesis processes.

Explanation

Due to its chemical properties and structure, the compound has potential uses in various fields, including medicinal chemistry, as a building block in the synthesis of more complex organic compounds, and as a reagent in various chemical reactions.

Explanation

The compound's structure consists of a benzene ring with two cyano groups (CN) at the 1 and 2 positions, an amino group (NH2) at the 4 position, and a bromo group (Br) at the 5 position. This structure contributes to its chemical properties and potential applications.

Derivative of benzenedicarbonitrile

Yes

Applications

Pharmaceutical synthesis, dye synthesis, and organic compound synthesis

Physical appearance

White to off-white powder

Solubility

Sparingly soluble in water, soluble in organic solvents

Potential applications

Medicinal chemistry, building block in organic synthesis, and as a reagent in chemical reactions

Chemical structure

Benzene ring with two cyano groups, an amino group, and a bromo group

Upstream product

• 206268-72-6 4-bromo-5-nitrophthalonitrile 
• 56765-79-8 3,4-dicyanoaniline 

Downstream Products

• 329308-83-0 4-acetylamino-5-bromophthalodinittrile 
• 329308-84-1 4-benzoylamino-5-bromophthalodinittrile 
• 655225-09-5 4-bromo-5-(4-undecyloxybenzoylamino)phthalonitrile 

Relevant academic research and scientific papers

Synthesis and Photophysical, Electrochemical and Theoretical Study of Thiazole-Annelated Phthalocyanines

Phthalocyanines with annelated thiazole rings were synthesised by cyclotetramerisation of benzothiazoledicarbonitriles. Three types of these dicarbonitriles with ortho-configuration were prepared from disubstituted anilines and their cyclisation led to al

IMIDAZO [4, 5 -C] PYRIDINE DERIVATIVES USEFUL FOR THE TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES

Novel imidazolopyridines according to Formula I, able to inhibit JAK are disclosed, wherein R1 and Cy are as disclosed herein. These compounds may be prepared as a pharmaceutical composition, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, allergic or inflammatory conditions, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6 or interferons.

Novel azo dye compound

A compound represented by formula (I): Formula (I) wherein Z1 and Z2 each are atoms necessary for forming an aromatic ring; V1 and V2 each are a substituent W1 or W2; when at least one V1 is W1, at least one V2 is W2, or when at least one V1 is W2, at least one V2 is W1; r is 1 to 4; s is 1 to 4; M1 is a counter ion; m1 is the number necessary for neutralizing charge; W1 is a hydroxyl, primary- or secondary- or tertiary-amino, acylamino, or sulfonamido group; W2 is a nitro, cyano, alkoxycarbonyl, aryloxycarbonyl, alkyl- or aryl-sulfonyl, carbamoyl, sulfamoyl, alkenyl, alkynyl, aryl, heterocyclic, sulfo, carboxyl, heterocyclic oxy, ammonio, alkyl- or aryl-sulfinyl, alkyl- or aryl-sulfonyl, acyl, or aryl- or heterocyclic-azo group; and the aromatic ring may have a substituent other than V1 and V2.

Tetraaminotetrabromo-and tetraacylaminotetrabromophthalocyanines

Reduction of the nitro group in 4-bromo-5-nitrophthalodinitrile gave 4-amino-5-bromophthalodinitrile. The latter was acylated to obtain 4-acetylamino-5-bromo- and 4-benzoylamino-5-bromophthalodinitriles which were used as starting materials for preparing