What is the (ETHYLTHIO)ACETONE?

(ETHYLTHIO)ACETONE is , while it's Molecular Formula is C5H10OS. Used in Chemical Synthesis: (Ethylthio)acetone is used as a reagent in chemical synthesis for its ability to detect, measure, or synthesize other substances. Its unique structure and properties make it a valuable component in various chemical reactions. Used in Research and Development: In the field of research and development, (ethylthio)acetone serves as a key compound for studying the properties and behavior of organosulfides and their potential applications in different industries. Used in Pharmaceutical Industry: (Ethylthio)acetone is used as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents. Used in Agrochemical Industry: In the agrochemical industry, (ethylthio)acetone may be utilized as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides, to improve crop protection and yield. Used in Material Science: (Ethylthio)acetone can be employed in material science for the development of new materials with unique properties, such as improved stability, reactivity, or selectivity in various applications.

What is the CAS number for (ETHYLTHIO)ACETONE?

The CAS number of (ETHYLTHIO)ACETONE is 20996-62-7.

What is (ETHYLTHIO)ACETONE (20996-62-7) used for?

(Ethylthio)acetone, also known as 1-(Ethylsulfanyl)propan-2-one, is a chemical compound belonging to the class of organic sulfur compounds, specifically organosulfides, which contain a sulfide group. With a molecular formula of C5H10OS and a molecular weight of 118.199 g/mol, it is primarily used as a reagent in the field of chemistry for detecting, measuring, or synthesizing other substances. Due to limited information on its properties, safety measures, or risks, it is crucial to handle (ETHYLTHIO)ACETONE with extreme caution and under the supervision of a trained professional.InChI:InChI=1/C5H10OS/c1-3-7-4-5(2)6/h3-4H2,1-2H3

What is the (ETHYLTHIO)ACETONE?

(ETHYLTHIO)ACETONE is , while it's Molecular Formula is C5H10OS. Used in Chemical Synthesis: (Ethylthio)acetone is used as a reagent in chemical synthesis for its ability to detect, measure, or synthesize other substances. Its unique structure and properties make it a valuable component in various chemical reactions. Used in Research and Development: In the field of research and development, (ethylthio)acetone serves as a key compound for studying the properties and behavior of organosulfides and their potential applications in different industries. Used in Pharmaceutical Industry: (Ethylthio)acetone is used as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents. Used in Agrochemical Industry: In the agrochemical industry, (ethylthio)acetone may be utilized as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides, to improve crop protection and yield. Used in Material Science: (Ethylthio)acetone can be employed in material science for the development of new materials with unique properties, such as improved stability, reactivity, or selectivity in various applications.

What is the CAS number for (ETHYLTHIO)ACETONE?

The CAS number of (ETHYLTHIO)ACETONE is 20996-62-7.

What is (ETHYLTHIO)ACETONE (20996-62-7) used for?

(Ethylthio)acetone, also known as 1-(Ethylsulfanyl)propan-2-one, is a chemical compound belonging to the class of organic sulfur compounds, specifically organosulfides, which contain a sulfide group. With a molecular formula of C5H10OS and a molecular weight of 118.199 g/mol, it is primarily used as a reagent in the field of chemistry for detecting, measuring, or synthesizing other substances. Due to limited information on its properties, safety measures, or risks, it is crucial to handle (ETHYLTHIO)ACETONE with extreme caution and under the supervision of a trained professional.InChI:InChI=1/C5H10OS/c1-3-7-4-5(2)6/h3-4H2,1-2H3

(ETHYLTHIO)ACETONE

Good factory supply good (ETHYLTHIO)ACETONE 20996-62-7

Molecular Formula: C5H10OS
Molecular Weight: 118.2
Vapor Pressure: 2.32mmHg at 25°C
Refractive Index: 1.4720
Boiling Point: 161 °C at 760 mmHg
Flash Point: 50.5 °C
PSA： 42.37000
Density: 0.967 g/cm³
LogP: 1.32850

(ETHYLTHIO)ACETONE(Cas 20996-62-7) Usage

General Description

(Ethylthio)acetone, also known under systematic name as 1-(Ethylsulfanyl)propan-2-one, is a chemical compound from the class of organic sulfur compounds, or specifically, organosulfides - a type of compounds containing a sulfide group. Its molecular formula is C5H10OS and the molecular weight is listed as 118.199 g/mol. It is most commonly used in the field of chemistry as a reagent, a substance used in chemical reactions to detect, measure, or synthesize other substances. Not much information is available about its exact properties, safety measures, or risks, emphasizing the necessity for handling such compound with extreme caution and under the supervision of a trained professional.

InChI:InChI=1/C5H10OS/c1-3-7-4-5(2)6/h3-4H2,1-2H3

20996-62-7 Relevant articles

METHOD FOR PRODUCING PYRIDINE COMPOUND

-

Paragraph 0260, (2020/01/24)

The present invention provides a method ...

Humicola lanuginosa lipase-catalyzed enantioselective resolution of β-hydroxy sulfides: Versatile synthons for enantiopure β-hydroxy sulfoxides

Singh, Satwinder,Kumar, Subodh,Chimni, Swapandeep Singh

, p. 2457 - 2462 (2007/10/03)

Humicola lanuginosa lipase-catalyzed acy...

Highly chemoselective α-diazo carbonyl insertion reactions into N-H and S-H bonds catalysed by [RuCl(η5-C5H5)(PPh3)2]

Del Zotto, Alessandro,Baratta, Walter,Rigo, Pierluigi

, p. 3079 - 3082 (2007/10/03)

Complex [RuCl(η5-C5H5)(PPh3)2], in chlor...

Sulfur substituted small-ring heterocycles

Zwanenburg,Philipse,Verstappen,Gieling

, p. 453 - 454 (2007/10/03)

The synthesis of epoxy sulfines and sulf...

20996-62-7 Process route

: 78-95-5
chloroacetone

: 75-08-1
ethanethiol

: 20996-62-7
1-(ethylthio)acetone

Conditions

Conditions	Yield
With potassium carbonate; Aliquat 336; In toluene; Ambient temperature;	85%
With sodium hydroxide;	84%
With hydrogenchloride; acetic acid;
With sodium; Yield given. Multistep reaction; 1) MeOH, 0 - 5 deg C, 30 min, 2) 0 - 5 deg C to room temperature, 30 min;
With sodium; In ethanol;
With sodium; In ethanol; for 2h;
With sodium hydroxide; In water; at 10 - 20 ℃; for 1h;