6285-66-1

Usage

Molecular structure

A complex organic compound with a phenyl ring, three hydroxyl groups, four carboxymethylsulfanyl groups, and a sulfanylacetic acid group.

Chelating properties

The presence of multiple carboxyl and sulfhydryl groups allows the compound to form stable complexes with metal ions.

Industrial applications

The compound may be used in various industrial processes due to its ability to sequester or bind to metals.

Pharmaceutical applications

2-[2,4,5-tris(carboxymethylsulfanyl)-3,6-dihydroxy-phenyl]sulfanylacetic acid may have potential therapeutic properties, making it useful in the pharmaceutical industry.

Antioxidant properties

The compound could exhibit antioxidant properties, which may help protect cells from damage caused by free radicals.

Versatility

2-[2,4,5-tris(carboxymethylsulfanyl)-3,6-dihydroxy-phenyl]sulfanylacetic acid has diverse applications in different fields, including chemistry, pharmaceuticals, and industry, due to its unique structure and properties.

Upstream product

• 68-11-1 mercaptoacetic acid 
• 106-51-4 p-benzoquinone 
• 7732-18-5 water 
• 118-75-2 chloranil 

Downstream Products

• 1413935-91-7 tetramethyl 2,2',2'',2'''-(3,6-dioxocyclohexa-1,4-diene-1,2,4,5-tetrayl)tetrakis(sulfanediyl)tetraacetate 
• 5657-46-5 (3,6-dioxo-cyclohexa-1,4-diene-1,2,4,5-tetrayltetramercapto)-tetra-acetic acid 

Relevant academic research and scientific papers

HIGH-AND LOW-POTENTIAL, WATER-SOLUBLE, ROBUST QUINONES

Substituted hydroquinones, 1,4-quinones, catechols, 1,2-quinones, anthraquinones, and anthrahydroquinones are disclosed herein. The substituted hydroquinones and catechols have the formula: while the substituted 1,4-quinones or 1,2-have the corresponding oxidized structure (1,4- benzoquinones and 1,2-benzoquinones). One or more of R1, R2, R3 and R4 include a sulfonate moiety, a sulfonimide moiety, or a phosphonate moiety, and any of R1, R2, R3 and R4 that do not include one of these moieties include an alkyl, a cycloalkyl, a thioether, a sulfoxide, a sulfone, a haloalkyl, a halogen, a nitrile, an imide, a pyrazole, or combinations thereof. The substituted anthraquinones have the formula: while the substituted anthrahydroquinones have the corresponding reduced structure. One or more of R1-R8 have a sulfonate or phosphate tethered to the ring by a thi other, amine, or ether including one or more alkyl groups. Any of R1-R8 that do not contain one of these moieties include an alkyl, a cycloalkyl, a thiother, a sulfoxide, a sulfone, a haloalkyl, a halogen, a hydroxyl, an alkoxyl, an ether, an amine, or hydrogen The substituted hydroquinones, 1,4-quinones, catechols, 1,2-quinones, anthraquinones, or anthrahydroquinones are soluble in water, stable in aqueous acid solutions, and have useful reduction potentials in the oxidized form. Accordingly, they can be used as redox mediators in emerging technologies, such as in mediated fuel cells or organic-mediator flow batteries.

Synthesis and photophysical study of an octahedral silver(I) 1-D coordination polymer with thiocarboxylic-acid-based ligands

We describe the synthesis of a unique 1-D silver coordination polymer, in which the silver metal center is, unusually, six-coordinated. The reaction of 2,3,5,6-tetrakis-(carboxymethylthio)-benzenediol (H2L) and AgNO3 in a 1:2 ratio r