4961-03-9

Basic information

• Product Name: 5-HYDROXYBENZENE-1,2,4-TRICARBOXYLIC ACID
• Synonyms: 5-HYDROXYBENZENE-1,2,4-TRICARBOXYLIC ACID;5-Hydroxy-1,2,4-benzenetricarboxylic acid;5-Hydroxybenzene-1,2,4-tricarboxylic acid, tech
• CAS NO: 4961-03-9
• Molecular Formula: C₉H₆O₇
• Molecular Weight: 226.14
• Mol File: 4961-03-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 543.5±50.0 °C(Predicted)
• Appearance: /
• Density: 1.802±0.06 g/cm3(Predicted)
• PKA: 2.10±0.10(Predicted)
• CAS DataBase Reference: 5-HYDROXYBENZENE-1,2,4-TRICARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-HYDROXYBENZENE-1,2,4-TRICARBOXYLIC ACID(4961-03-9)
• EPA Substance Registry System: 5-HYDROXYBENZENE-1,2,4-TRICARBOXYLIC ACID(4961-03-9)

Safety Data

• Hazardous Substances Data: 4961-03-9(Hazardous Substances Data)

Usage

Chemical Structure

It consists of a benzene ring with three carboxylic acid groups ( -\textCOOH ) and a hydroxyl group ( -\textOH ) attached.

Applications

Synthesis of Metal-Organic Frameworks (MOFs): Used in the production of porous materials with applications in catalysis, gas storage, and separation.
Polymer Production: Utilized in the manufacturing of polymers.
Precursor for Pharmaceuticals and Agrochemicals: Serves as a starting material for the synthesis of various pharmaceutical and agrochemical compounds.

Versatility

Trimesic acid exhibits versatility in both industrial and research domains.

Upstream product

• 3453-84-7 2,4,5-trimethylbenzenesulfonic acid 
• 95-63-6 1,2,4-Trimethylbenzene 
• 51307-74-5 5-sulfonyl-1,2,4-benzenetricarboxylic acid 
• 13124-84-0 5-bromobenzene-1,2,4-tricarboxylic acid 
• 5469-19-2 1-bromo-2,4,5-trimethylbenzene 

Downstream Products

• 32136-60-0 methyl 5-methoxytrimellitate 
• 114930-83-5 5-hydroxy-6-nitro-benzene-1,2,4-tricarboxylic acid trimethyl ester 
• 124-38-9 carbon dioxide 
• 99-06-9 3-Carboxyphenol 
• 108-95-2 phenol 
• 52060-72-7 5-methoxy-benzene-1,2,4-tricarboxylic acid 

Relevant articles and documents

PFKFB3 INHIBITORS AND THEIR USES

This disclosure relates to new phthalimide and isoindolinone derivatives and other PFKFB3 inhibitors for use in the treatment of diseases. The invention further relates to pharmaceutical compositions containing such PFKFB3 inhibitors, methods of preparation thereof, methods for their use as therapeutic agents, and methods of preparation of a medicament for use in therapy, as well as kits and other inventiions comprising such PFKFB3 inhibitors. These PFKFB3 inhibitors are useful for the treatment and prophylaxis of cancer, neurodegenerative diseases, autoimmune diseases, inflammatory disorders, multiple sclerosis, metabolic diseases, inhibition of angiogenesis and other diseases and conditions, where the modulation of PFKFB3 and/or PFKFB4 has beneficial effect as well as neuroprotection.

Inclusion complex containing epoxy resin composition for semiconductor encapsulation

The invention is an epoxy resin composition for sealing a semiconductor, including (A) an epoxy resin and (B) a clathrate complex. The clathrate complex is one of (b1) an aromatic carboxylic acid compound, and (b2) at least one imidazole compound represented by formula (II): wherein R2 represents a hydrogen atom, C1-C10 alkyl group, phenyl group, benzyl group or cyanoethyl group, and R3 to R5 represent a hydrogen atom, nitro group, halogen atom, C1-C20 alkyl group, phenyl group, benzyl group, hydroxymethyl group or C1-C20 acyl group. The composition has improved storage stability, retains flowability when sealing, and achieves an effective curing rate applicable for sealing delicate semiconductors.