208243-72-5

Usage

Uses

Used in Pharmaceutical Industry:
1,2-Dithiolane-4-carboxylic acid, 4-methylis used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with improved therapeutic properties and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, 1,2-Dithiolane-4-carboxylic acid, 4-methylserves as a crucial building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness and selectivity, leading to more sustainable agricultural practices.
Used in Organic Synthesis:
1,2-Dithiolane-4-carboxylic acid, 4-methylis used as a versatile building block in organic synthesis. Its carboxylic acid and methyl groups can be further modified or functionalized to create a wide range of sulfur-containing organic compounds with potential applications in various industries.
Used in Material Science:
Due to its unique structure and properties, 1,2-Dithiolane-4-carboxylic acid, 4-methylhas potential applications in the development of new materials with specific properties, such as improved thermal stability, chemical resistance, or biocompatibility. These materials can be used in various applications, including coatings, adhesives, and polymers.

InChI:InChI=1/C5H8O2S2/c1-5(4(6)7)2-8-9-3-5/h2-3H2,1H3,(H,6,7)

Upstream product

• 64855-18-1 3,3-dichloro-2,2-dimethylpropionic acid 
• 67329-11-7 2,2-bis(chloromethyl)propanoic acid 

Downstream Products

• 208243-73-6 4-methyl-1,2-dithiolane-4-carboxamide 

Relevant academic research and scientific papers

Stereodivergent Chirality Transfer by Noncovalent Control of Disulfide Bonds

Controlling dynamic stereochemistry is an important challenge, as it is not only inherent to protein structure and function but often governs supramolecular systems and self-assembly. Typically, disulfide bonds exhibit stereodivergent behavior in proteins

TRIPODAL SQUARAMIDE-BASED MONOMERS

The present invention relates to a tripodal squaramide-based monomer based monomer according to formula (I) for the formation of supramolecular polymers: wherein T represents a central atom; n is an integer of from 4 to 12; and R1 is a group ac

Cosmetic/sunscreen compositions containing dibenzoylmethane compounds and dithiolane compound photostabilizers therefor

Cosmetic/sunscreen compositions contain a combination of at least one dibenzoylmethane sunscreen compound and a photostabilizing amount of at least one dithiolane compound of formula (I) below:

Depigmenting keratin materials utilizing dithiolane compounds

A cosmetic regime or regimen for depigmenting, lightening and/or bleaching keratin materials, especially the skin, entails topically applying thereon a cosmetic composition containing a dithiolane compound of formula (I): in which: Y is O, NR1 or SR1 is a hydrogen atom; a C1-C20 alkyl radical or an optionally substituted phenyl radical;R is a hydrogen atom; or a C1-C20 alkyl radical, or an optionally substituted phenyl radical, or a C1-C8 alkyl radical containing an optionally substituted phenyl substituent;n=0 or 1 or 2; and also the salts, chelates, solvates and optical isomers thereof.

Administration of dithiolane compounds for photoprotecting the skin

Dithiolane compounds having the structural formula (I): are useful for reinforcing and/or preserving the natural antioxidant protection of the skin against oxidative stress caused, especially, by UV radiation, e.g., by increasing the level of intracellular glutathione.