17640-29-8

Basic information

• Product Name: Acetic acid, (ethylthio)-, ethyl ester
• Synonyms: Ethyl ethylsulfenylacetate;NSC 509544;Acetic acid, (ethylthio)-, ethyl ester
• CAS NO: 17640-29-8
• Molecular Formula: C₆H₁₂O₂S
• Molecular Weight: 148.22328
• Mol File: 17640-29-8.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 101-102℃ (5 Torr)
• Flash Point: 69°C
• Appearance: /
• Density: 1.022g/cm³
• Vapor Pressure: 0.793mmHg at 25°C
• Refractive Index: 1.4575 (589.3 nm 20℃)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Acetic acid, (ethylthio)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, (ethylthio)-, ethyl ester(17640-29-8)
• EPA Substance Registry System: Acetic acid, (ethylthio)-, ethyl ester(17640-29-8)

Safety Data

• Hazardous Substances Data: 17640-29-8(Hazardous Substances Data)

Usage

General Description

Acetic acid, (ethylthio)-, ethyl ester is a chemical compound with the formula C6H12O2S. It is also known as ethyl ethanethioate and is a colorless liquid with a pungent odor. It is commonly used as a flavoring agent and in the production of various industrial and consumer products, including perfumes and pharmaceuticals. The compound is also used as a solvent and as an intermediate in the synthesis of other chemicals. It is important to handle this compound with care, as it can be irritating to the skin and eyes, and may have harmful effects if ingested or inhaled.

InChI:InChI=1/C6H12O2S/c1-3-8-6(7)5-9-4-2/h3-5H2,1-2H3

Upstream product

• 463-51-4 Ketene 
• 1496-75-9 Ethanesulfenyl chloride 
• 352-93-2 diethyl sulphide 
• 105-36-2 ethyl bromoacetate 
• 682-91-7 ethyl ethanethiosulfonate 
• 927-80-0 1-ethoxyacetylene 
• 75-08-1 ethanethiol 
• 75-03-6 ethyl iodide 
• 623-51-8 ethyl 2-sulfanylacetate 
• 105-39-5 chloroacetic acid ethyl ester 
• 64-17-5 ethanol 
• 91418-07-4 chloro(ethylsulfanyl)acetylene 
• 74-96-4 ethyl bromide 
• 623-73-4 diazoacetic acid ethyl ester 

Downstream Products

• 85677-86-7 2-(ethylthio)acetohydrazide 
• 60775-13-5 α-Benzyliden-S-aethylthioglykollsaeure 
• 627-04-3 S-ethylthioglycolic acid 

Relevant articles and documents

Design, synthesis and bioactivity evaluation of novel thioether derivatives containing a sulfonohydrazide moiety

A series of novel thioether derivatives containing a sulfonohydrazide moiety were synthesized and determined using 1H NMR, 13C NMR, HRMS, and elemental analysis. Their in vitro antibacterial activities against Xanthomonas oryzae pv.

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.

N-ALKYNYL-2- (SUBSTITUTED ARYLOXY) ALKYLTHIOAMIDE DERIVATIVES AS FUNGICIDES

Fungicidal compounds of the general formula (1), wherein Ar is a group of the formula (A), (B1), (B2) or (C), or Ar is a 5- or 6-linked group of the formula (D1) or (D2); and R1, R2, R3, R4, R5, n, A1, A2, A3, A4, A5, Ka, Kb, L, M, V, W, X,Y and Z have the definitions given in claim 1.