627-04-3

Usage

Uses

Used in Pharmaceutical Industry:
(Ethylthio)acetic Acid is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its presence of sulfur makes it an excellent nucleophile, participating in chemical reactions that facilitate the production of certain drugs.
Used in Agrochemical Industry:
(Ethylthio)acetic Acid is used as a component in the formulation of agrochemicals. Its reactivity and sulfur content contribute to the development of effective products for agricultural applications.
Used in Dye Industry:
(Ethylthio)acetic Acid is used as a raw material in the production of dyes. The unique properties of (ETHYLTHIO)ACETIC ACID, including its sulfur atom, enable the creation of a wide range of colorants for various industries.

InChI:InChI=1/C4H8O2S/c1-2-7-3-4(5)6/h2-3H2,1H3,(H,5,6)

Upstream product

• 53250-09-2 2-(ethylthio)acetonitrile 
• 3926-62-3 sodium monochloroacetic acid 
• 811-51-8 sodium thioethylate 
• 74-96-4 ethyl bromide 
• 68-11-1 mercaptoacetic acid 
• 563-17-7 potassium ethyl sulfate 
• 79-11-8 chloroacetic acid 
• 75-08-1 ethanethiol 
• 17640-29-8 ethyl 2-(ethylthio)acetate 
• 36638-31-0 1,1,2-tris-ethylsulfanyl-ethene 
• 1071-37-0 2-ethylisothiourea hydrobromide 
• 4841-22-9 (4-chloro-phenoxy)-acetic acid methyl ester 
• 75-03-6 ethyl iodide 
• 105-39-5 chloroacetic acid ethyl ester 

Downstream Products

• 81221-65-0 N,N'-bis-(toluene-4-sulfonyl)-ethanesulfinamidyne 
• 57830-38-3 ethanesulfinyl-acetic acid 
• 141811-44-1 2-(ethanesulfonyl)acetic acid 
• 60247-87-2 ethylsulfanyl-acetic acid amide 
• 20600-64-0 methyl ethylsulfenylacetate 
• 30506-11-7 Dibromomethyl ethyl sulfon 
• 27850-41-5 Phenyl-aethylthioacetat 
• 22132-08-7 Ethylmercaptoessigsaeure-o-nitro-phenylester 
• 58992-39-5 (C₆H₅)3Bi(OOCCH₂SC₂H₅)2 
• 636-70-4 triethylamine hydrobromide 
• 339983-71-0 C₆H₅Pd(P(C₆H₅)3)2OCOCH₂SCH₂CH₃ 
• 1132700-54-9 N-[2-chloro-4-[5-(3,4,5-trichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]phenyl]methyl-2-ethylthio-N-methylacetamide 
• 1132699-40-1 N-[4-[5-[3,5-bis(trifluoromethyl) phenyl]-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl] phenyl] [cyano] methyl-2-(ethylthio) acetamide 
• 1444176-48-0 N-[[4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methylphenyl]methyl]-N-ethyl-2-ethylsulfanylacetamide 

Relevant academic research and scientific papers

HETEROCYCLIC AMIDE COMPOUND

PROBLEM TO BE SOLVED: To provide a heterocyclic amide compound useful as an active ingredient of a herbicide. SOLUTION: The present disclosure provides a heterocyclic amide compound represented by the following formula or a salt thereof. Q-N(R3)-C(=X)-W (Q: a substituted/unsubstituted 1,3,4-oxadiazole, 1,2,5-oxadiazole or the like. W: a substituted/unsubstituted [1,2,4]triazolo[4,3-a]pyridine or the like. X: O, S. R3: H, C1-C6 alkyl or the like). SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

HETEROCYCLIC AMIDE COMPOUND

PROBLEM TO BE SOLVED: To provide a herbicide that reliably has an effect on various weeds at a reduced dosage, has reduced trouble such as soil pollution and influence on succeeding crops, and is highly safe. SOLUTION: The present invention provides a heterocyclic amide compound represented by the following formula and a herbicide containing the same. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

HETEROCYCLIC AMIDO COMPOUND

PROBLEM TO BE SOLVED: To provide a novel pesticide, especially a herbicide. SOLUTION: There are provided a heterocycle amide compound such as 3-isopropyl-N-(5-methyl-1, 3, 4-oxadiazole-2-yl)-5-(trifluoromethyl)-[1, 2, 4]triazolo [4,3-a] pyridine-8-carboxamide (compound No.1-004), 3-isopropyl-N-(5-methyl-1, 3, 4-oxadiazole-2-yl)-5-(methylthio)-[1,2,4] triazolo [4,3-a] pyridine-8-carboxamide (compound No.1-009), and a herbicide containing them. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

COMPOSITIONS, SYNTHESIS, AND METHODS OF USING PHENYLCYCLOALKYLMETHYLAMINE DERIVATIVES

The present invention provides novel phenylcycloalkylmethylamme derivatives, and methods of preparing phenylcycloalkylmethylamme derivatives. The present invention also provides methods of using phenylcycloalkylmethylamme derivatives and compositions of phenylcycloalkylmethylamme derivatives. The pharmaceutical compositions of the compounds of the present invention can be used for treating and/or preventing obesity and obesity related co- morbid indications and depression and depression related co-morbid indications.

3-Thiolated 2-azetidinones: Synthesis and in vitro antibacterial and antifungal activities

A series of 3-thiolated β-lactams were synthesized by [2+2] ketene-imine cycloaddition reaction from S-substituted mercaptoacetic acids and Schiff bases. Then, some of the 3-methylthio β-lactams were converted to 3-(methylsulfinyl) β-lactams and 3-(methylsulfonyl) β-lactams using m-CPBA under different reaction conditions. All the compounds were characterized by spectral data and elemental analyses and were evaluated for their in vitro antibacterial and antifungal activities against pathogenic strains including Staphylococcus aureus (Methicillin resistant strain). The preliminary screening results indicated that some of these compounds demonstrated moderate to very good antibacterial and antifungal activities.

Studies on umami taste. Synthesis of new guanosine 5′-phosphate derivatives and their synergistic effect with monosodium glutamate

A number of N2-alkyl and N2-acyl derivatives of guanosine 5′-phosphate (GMP) have been synthesized and tested for their synergistic effect with monosodium L-glutamate (MSG), the prototypical substance imparting umami taste to savory-based foods. Capacities to enhance the taste intensity of MSG (γ values) were estimated through subjective comparisons of MSG/nucleotide mixtures in water with appropriate solutions of MSG alone. Assuming β = γ[nucleotide]/γ[IMP], β values of the N 2-substituted GMPs were found in the range 1.2-5.7. Such values appear to be related to the chain length of the substituent in the 2-position of the purine nucleus and dependent on the replacement of a CH2 group with an S atom and/or with an α-CO group. These findings indicate that the exocyclic NHR group of the guanine moiety is actively implicated in the synergism between GMP derivatives and MSG. Theoretical calculations suggest that an anti conformation is probably assumed by ribonucleotide molecules interacting with umami receptors.

Sulfonyl Esters. V. A Preparation of Dichloromethyl Sulfones

α-Sulfonyl methyl esters have been chlorinated in the presence of base.Chlorination proceeds with accompanying demethoxycarbonylation to furnish dichloromethyl sulfones in good yields.

Process for preparing thioethers of mercapto-acids

A process for preparing thioethers of mercaptocarboxylic acids by contacting glycolic acid or bromoacetic acid and a mercaptan in the presence of aqueous hydrogen bromide.