51762-85-7

Usage

Chemical structure

A benzene ring with two carboxylic acid groups and a thioether group attached at the 2-position.

Molecular weight

294.34 g/mol.

Functional groups

Carboxylic acid, thioether, and aromatic ring.

Appearance

Solid or crystalline form.

Solubility

Soluble in organic solvents such as ethanol, methanol, and acetone.

Stability

Stable under normal temperature and pressure conditions.

Reactivity

Reacts with various reagents to form different organic compounds and polymers.

Applications

Used as a building block in the synthesis of various organic compounds and polymers, with potential applications in pharmaceuticals, dyes, and plastics industries.

Potential uses

Drug development and material science due to its unique structural features and properties.

Synthesis

The synthesis and properties make it a valuable and versatile chemical in various industrial processes and research applications.

Upstream product

• 5292-45-5 dimethyl 2-nitroterephthalate 
• 106-45-6 para-thiocresol 

Downstream Products

• 51763-07-6 7-methyl-9-oxothioxanthene-3-carboxylic acid 

Relevant academic research and scientific papers

LOW-EXTRACTABLE THIOXANTHONES

3-Esters and 3-amides of thioxanthone bearing alkyl chains of appropriate length and can be used as photoinitiators or sensitizers in photopolymerizable systems, in particular for the preparation of coatings compatible with the food use.

Thioxanthonecarboxylic acid esters, thioesters and amides

Thioxanthonecarboxylic acid esters, thioesters or amides of the formula I STR1 in which X and Z are hydrogen or one of the substituents defined in more detail in claim 1 and Y is --OR1, --SR1 or --N(R1)(R2), in

Thioxanthonecarboxylic acids, esters, thioesters and amides with reactive functional groups

Thioxanthone carboxylic acid esters, thioesters and amides with reactive functional groups of the formula STR1 in which X, Y, Z, n and Q are as defined in the patent claim and Q is, for example, --OCH=CH2, --OCH2 CH=CH2, -

Antiallergic cyclic sulphur compounds

Certain tricyclic thioxanthone-10,10-dioxide compounds each of which is substituted in the 1-,2-,3- or 4-position by a carboxyl or (5-tetrazolyl) group and each of which is optionally substituted in the 5-,6-,7- or 8-position by a second carboxyl or (5-tetrazolyl) group or a substituent selected from cyano, halogen, nitro, alkyl, alkoxy, acyl, amino, acylamino, thioalkyl, alkylsulphinyl and alkylsulphonyl, as well as salts, and optionally substituted esters and amides of the carboxyl substituted compounds and alkyl derivatives of the tetrazolyl substituted compounds, are useful for the relief or prophylaxis of allergic conditions.

Cyclic sulphur compounds

Certain tricyclic thioxanthone-10,10-dioxide compounds each of which is substituted in the 1-,2-,3- or 4-position by a carboxyl or (5-tetrazolyl) group and each of which is optionally substituted in the 5-,6-,7- or 8-position by a second carboxyl or (5-tetrazolyl) group or a substituent selected from cyano, halogen, nitro, alkyl, alkoxy, acyl, amino, acylamino, thioalkyl, alkylsulphinyl and alkylsulphonyl, as well as salts, and optionally substituted esters and amides of the carboxyl substituted compounds and alkyl derivatives of the tetrazolyl substituted compounds, are useful for the relief or prophylaxis of allergic conditions.