1583-65-9

Basic information

• Product Name: 2-fluoroisophthalic acid
• Synonyms: 2-fluoroisophthalic acid;2-fluorobenzene-1,3-dicarboxylic acid;2-fluoro-1,3-Benzenedicarboxylic acid;2-fluorobenzene-1,3-dicarboxylic aci
• CAS NO: 1583-65-9
• Molecular Formula: C₈H₅FO₄
• Molecular Weight: 184.1213032
• Mol File: 1583-65-9.mol
• Article Data: 6

Chemical Properties

• Melting Point: 286-287 °C
• Boiling Point: 393.6±27.0 °C(Predicted)
• Appearance: /
• Density: 1.551±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 2.60±0.10(Predicted)
• CAS DataBase Reference: 2-fluoroisophthalic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-fluoroisophthalic acid(1583-65-9)
• EPA Substance Registry System: 2-fluoroisophthalic acid(1583-65-9)

Safety Data

• Hazardous Substances Data: 1583-65-9(Hazardous Substances Data)

Usage

General Description

2-Fluoroisophthalic acid is a chemical compound with the molecular formula C8H5FO4. It is a derivative of isophthalic acid, with a fluorine atom attached to the second carbon of the benzene ring. 2-fluoroisophthalic acid is used in the production of pharmaceuticals, agrochemicals, and functional materials. It is also used as a building block in the synthesis of various organic compounds. 2-Fluoroisophthalic acid has potential applications in the fields of biotechnology, materials science, and drug development due to its unique chemical properties and reactivity. It is also a valuable intermediate in the synthesis of fluorescent dyes and polymers.

Upstream product

• 443-88-9 2-fluoro-m-xylene 
• 21161-11-5 2-nitroisophthalic acid 
• 723334-03-0 2-fluoro-isophthalic acid dimethyl ester 
• 91129-30-5 2-fluoroisophthalic acid dichloride 
• 81-20-9 2,6-dimethylnitrobenzene 
• 87-62-7 2,6-dimethylaniline 

Downstream Products

• 640768-78-1 2-fluoroisophthalic acid monooctyl ester 
• 723334-03-0 2-fluoro-isophthalic acid dimethyl ester 
• 914301-44-3 2-fluoroisophthalic acid monomethyl ester 
• 914301-45-4 2-fluoro-5-nitroisophthalic acid monomethyl ester 
• 914301-49-8 2-fluoro-3-(4-methoxybenzyl)-5-nitrobenzaldehyde 
• 914301-48-7 [2-fluoro-3-(4-methoxybenzyl)-5-nitrophenyl]methanol 
• 914301-47-6 2-fluoro-3-(4-methoxybenzyl)-5-nitrobenzoic acid methyl ester 
• 914301-46-5 2-fluoro-3-(4-methoxybenzoyl)-5-nitrobenzoic acid methyl ester 
• 914301-58-9 2-[2-fluoro-3-(4-methoxy-benzyl)-5-nitro-benzylamino]-ethanol 
• 914301-50-1 [2-(tert-butyldimethylsilanyloxy)ethyl]-[2-fluoro-3-(4-methoxybenzyl)-5-nitrobenzyl]amine 
• 869203-28-1 N,N'-bis-(3-amino-5-dioctylcarbamoyl-2-fluoro-phenyl)-2-fluoro-isophthalamide 
• 723334-05-2 2-(4-formylphenoxy)-isophthalic acid dimethyl ester 
• 1041480-58-3 2-{4-[2-(4-iodophenyl)vinyl]phenoxy}-isophthalic acid dimethyl ester 
• 1041480-59-4 2-{4-[2-(4-iodophenyl)vinyl]phenoxy}-isophthalic acid 

Relevant articles and documents

Potent non-benzoquinone ansamycin heat shock protein 90 inhibitors from genetic engineering of Streptomyces hygroscopicus

Inhibition of the protein chaperone Hsp90 is a promising new approach to cancer therapy. We describe the preparation of potent non-benzoquinone ansamycins. One of these analogues, generated by feeding 3-amino-5-chlorobenzoic acid to a genetically engineer

Macrolactams by engineered biosynthesis

Macrolactams are made by feeding aromatic amino acids as replacement starter units to a mutant strain of the geldanamycin-producing microorganism Streptomyces hygroscopicus var. geldanus NRRL 3602, wherein the gene cluster encoding enzymes for the biosynt

A lockable light-driven molecular shuttle with a fluorescent signal

A turn on! A lockable photodriven molecular shuttle is based on a [2]rotaxane that consists of an α-cyclodextrin threaded by a stilbene derivative. The fluorescent signals originate from the naphthalimide stopper and indicate the position of the shuttle. Once unlocked, the device can be turned on by irradiation at 335 nm and turned off by irradiation at 280 nm. The shuttle can be locked or unlocked by the addition acid or alkali, respectively (see picture).