35040-68-7

Usage

Uses

Used in Organic Synthesis:
2,2-dimethyl-3-sulfanylpropanoic acid is utilized as a precursor in organic synthesis, serving as a key building block for the creation of more complex organic molecules. Its presence in the synthesis process is crucial for the development of a wide range of chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,2-dimethyl-3-sulfanylpropanoic acid is used as a building block for the production of various drugs. Its unique structure allows it to be incorporated into the molecular frameworks of different medicinal compounds, contributing to their therapeutic properties.
Used in Agrochemicals:
2,2-dimethyl-3-sulfanylpropanoic acid also plays a role in the agrochemical sector, where it is used as a component in the synthesis of various agrochemical products. Its contribution to the development of these products helps address agricultural needs such as pest control and crop protection.
Used as a Flavoring Agent:
2,2-dimethyl-3-sulfanylpropanoic acid has been studied for its potential application as a flavoring agent. Its unique chemical properties may contribute to the development of new flavors or enhance existing ones in the food and beverage industry.
Used in the Chemical Industry for Sulfur-Containing Compounds:
As an important intermediate in the synthesis of various sulfur-containing compounds, 2,2-dimethyl-3-sulfanylpropanoic acid is of significant interest to the chemical industry. Its role in the production of these compounds highlights its importance in advancing the capabilities and applications of sulfur chemistry.

Upstream product

• 2843-17-6 3-bromo-2,2-dimethylpropionic acid 
• 959762-95-9 4-amino-6-{7-chloro-3-oxatricyclo[7.3.1.0^5,13]trideca-1⁽¹³⁾,5,7,9,11-pentaen-8-yl}-1,3,5-triazine-2-thiol 
• 13511-38-1 3-chloropivalic acid 
• 4835-90-9 3-Hydroxy-2,2-dimethylpropanoic acid 

Downstream Products

• 1025806-94-3 3-(4-Methoxy-benzylsulfanyl)-2,2-dimethyl-propan-1-ol 
• 151826-26-5 3-(4-methoxybenzylthio)-2,2-dimethylpropanal 
• 151826-30-1 N-<3-(4-methoxybenzylthio)-2,2-dimethylpropyl>-L-cysteine methyl ester 
• 140691-71-0 methyl (4R)-3-<3-(4-methoxybenzylthio)-2,2-dimethylpropyl>-2-thioxothiazolidine-4-carboxylate 
• 89024-21-5 1,3,3-trimethyl-4-phenylthioazetidin-2-one 
• 89024-20-4 N-2,2-trimethyl-3-(phenylthio)-propionamide 
• 97759-70-1 3-chloro-N,2,2-trimethyl-3-phenylthiopropionamide 
• 128620-82-6 SA₃₄₄₃ 
• 137190-59-1 3-(4-Methoxy-benzylsulfanyl)-2,2-dimethyl-propionic acid 

Relevant academic research and scientific papers

Design and synthesis of 2-amino-6-(1H,3H-benzo[de]isochromen-6-yl)-1,3,5- triazines as novel Hsp90 inhibitors

A novel series of 2-amino-1,3,5-triazines bearing a tricyclic moiety as heat shock protein 90 (Hsp90) inhibitors is described. Molecular design was performed using X-ray cocrystal structures of the lead compound CH5015765 and natural Hsp90 inhibitor geldanamycin with Hsp90. We optimized affinity to Hsp90, in vitro cell growth inhibitory activity, water solubility, and liver microsomal stability of inhibitors and identified CH5138303. This compound showed high binding affinity for N-terminal Hsp90α (Kd = 0.52 nM) and strong in vitro cell growth inhibition against human cancer cell lines (HCT116 IC50 = 0.098 μM, NCI-N87 IC50 = 0.066 μM) and also displayed high oral bioavailability in mice (F = 44.0%) and potent antitumor efficacy in a human NCI-N87 gastric cancer xenograft model (tumor growth inhibition = 136%).

Synthesis and pharmacological activities of novel cyclic disulfide and cyclic sulfide derivatives as hepatoprotective agents

In order to search for anti-hepatitis drugs, we synthesized a series of eight- and nine-membered cyclic disulfides (1) and six- and seven-membered cyclic sulfides (2) and evaluated them for ability to reduce mortality in the model of acute hepatic failure

Pyridylthio-acylanilide herbicides

Novel herbicidally active pyridylthio-acylanilides of the formula STR1 in which R1, R2 and R3, independently of one another, represent hydrogen, halogen, cyano or trifluoromethyl or alkyl, alkoxy and alkylthio having 1 to 4 carbon atoms in each case, R4 represents halogen, methyl or methoxy, n represents a number 0, 1 or 2, z represents the group (Ia) STR2 or the group (Ib) STR3 where X represents oxygen, sulphur, an N--R10 or N--O--R11 group, or X and Rg tpgether represent the STR4 radical, and the other radicals can have various meanings. Intermediates of the formulae STR5 are also new.