What is the 2,2,2-trifluoroethanethioamide?

2,2,2-trifluoroethanethioamide is , while it's Molecular Formula is C2H2 F3 N S. Used in Organic Synthesis: 2,2,2-Trifluoroethanethioamide serves as a source of nucleophilic 2,2,2-trifluoroethylthio anion, which is capable of participating in a variety of chemical reactions. Its reactivity and the presence of fluorine atoms make it a valuable intermediate in the synthesis of complex organic molecules. Used in Pharmaceutical Synthesis: In the pharmaceutical industry, 2,2,2-trifluoroethanethioamide is utilized as a building block for the synthesis of various drugs. Its unique chemical properties allow for the creation of novel therapeutic agents with potential applications in treating a range of medical conditions. Used in Agrochemical Synthesis: Similarly, in the agrochemical sector, 2,2,2-trifluoroethanethioamide is employed as a key component in the development of new pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness and selectivity, contributing to more efficient and sustainable agricultural practices. Overall, the diverse applications of 2,2,2-trifluoroethanethioamide across different industries highlight its importance as a chemical intermediate and building block, underpinning its value in modern chemical research and development.

What is the CAS number for 2,2,2-trifluoroethanethioamide?

The CAS number of 2,2,2-trifluoroethanethioamide is 421-52-3.

What is 2,2,2-trifluoroethanethioamide (421-52-3) used for?

2,2,2-Trifluoroethanethioamide, also known as trifluoroethyl thioacetamide, is a chemical compound characterized by the molecular formula C4H6F3NS. It is a thioamide derivative distinguished by the presence of three fluorine atoms attached to a carbon atom and a sulfur atom bonded to the nitrogen atom. This unique structure endows 2,2,2-trifluoroethanethioamide with specific chemical properties and reactivity, making it a versatile compound in various chemical and industrial applications.InChI:InChI=1/C2H2F3NS/c3-2(4,5)1(6)7/h(H2,6,7)

What is the 2,2,2-trifluoroethanethioamide?

2,2,2-trifluoroethanethioamide is , while it's Molecular Formula is C2H2 F3 N S. Used in Organic Synthesis: 2,2,2-Trifluoroethanethioamide serves as a source of nucleophilic 2,2,2-trifluoroethylthio anion, which is capable of participating in a variety of chemical reactions. Its reactivity and the presence of fluorine atoms make it a valuable intermediate in the synthesis of complex organic molecules. Used in Pharmaceutical Synthesis: In the pharmaceutical industry, 2,2,2-trifluoroethanethioamide is utilized as a building block for the synthesis of various drugs. Its unique chemical properties allow for the creation of novel therapeutic agents with potential applications in treating a range of medical conditions. Used in Agrochemical Synthesis: Similarly, in the agrochemical sector, 2,2,2-trifluoroethanethioamide is employed as a key component in the development of new pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness and selectivity, contributing to more efficient and sustainable agricultural practices. Overall, the diverse applications of 2,2,2-trifluoroethanethioamide across different industries highlight its importance as a chemical intermediate and building block, underpinning its value in modern chemical research and development.

What is the CAS number for 2,2,2-trifluoroethanethioamide?

The CAS number of 2,2,2-trifluoroethanethioamide is 421-52-3.

What is 2,2,2-trifluoroethanethioamide (421-52-3) used for?

2,2,2-Trifluoroethanethioamide, also known as trifluoroethyl thioacetamide, is a chemical compound characterized by the molecular formula C4H6F3NS. It is a thioamide derivative distinguished by the presence of three fluorine atoms attached to a carbon atom and a sulfur atom bonded to the nitrogen atom. This unique structure endows 2,2,2-trifluoroethanethioamide with specific chemical properties and reactivity, making it a versatile compound in various chemical and industrial applications.InChI:InChI=1/C2H2F3NS/c3-2(4,5)1(6)7/h(H2,6,7)

Reputable factory supply 2,2,2-trifluoroethanethioamide 421-52-3 in stock with high standard

Product Details;

CasNo： 421-52-3

MF： C2H2 F3 N S

Reputable factory supply 2,2,2-trifluoroethanethioamide 421-52-3 in stock with high standard

Molecular Formula:C2H2 F3 N S
Molecular Weight:129.106
Vapor Pressure:31.5mmHg at 25°C
Melting Point:42-43 °C(Solv: ethyl ether (60-29-7))
Refractive Index:1.434
Boiling Point:104°Cat760mmHg
PKA:11.02±0.29(Predicted)
Flash Point:16.7°C
PSA：58.11000
Density:1.49g/cm³
LogP:1.53510

2,2,2-trifluoroethanethioamide(Cas 421-52-3) Usage

General Description

2,2,2-trifluoroethanethioamide, also known as trifluoroethyl thioacetamide, is a chemical compound with the molecular formula C4H6F3NS. It is a thioamide derivative with three fluorine atoms attached to the carbon atom and a sulfur atom bonded to the nitrogen atom. 2,2,2-trifluoroethanethioamide is used in organic synthesis as a source of nucleophilic 2,2,2-trifluoroethylthio anion, which can participate in a variety of reactions. Additionally, it is also used as a building block for the synthesis of pharmaceuticals and agrochemicals. This chemical has a wide range of industrial applications due to its unique chemical properties and reactivity.

InChI:InChI=1/C2H2F3NS/c3-2(4,5)1(6)7/h(H2,6,7)

421-52-3 Relevant articles

Cycloaddition reactions of polyfluoroalkylthioncarboxylic acid derivatives with dimethyl acetylenedicarboxylate (DMAD)

Rudnichenko,Timoshenko,Shermolovich

, p. 439 - 444 (2004)

Polyfluoroalkyldithiocarboxylates react ...

Compound synthesized from new thiazole monomer including electron withdrawing group and manufacturing method thereof

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Paragraph 0116-0121, (2019/10/08)

The present invention relates to a compo...

HETEROARYL SUBSTITUTED BETA-HYDROXYETHYLAMINES FOR USE IN TREATING HYPERGLYCAEMIA

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Page/Page column 47, (2019/04/11)

There is herein provided a compound of f...

SUBSTITUTED OXAZOLE- AND THIAZOLE-BASED CARBOXAMIDE AND UREA DERIVATIVES AS VANILLOID RECEPTOR LIGANDS II

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Paragraph 21-22, (2016/06/14)

The invention relates to oxazole and thi...

BENZPYRAZOL DERIVATIVES AS INHIBITORS OF PI3 KINASES

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Page/Page column 109-110, (2009/12/28)

The invention is directed to certain nov...

421-52-3 Process route

: 354-38-1
2,2,2-trifluoroacetamide

: 421-52-3
trifluorothioacetamide

Conditions

Conditions	Yield
With tetraphosphorus decasulfide; In tetrahydrofuran; at 70 - 75 ℃; for 4h; Inert atmosphere;	95%
With Lawessons reagent; In tetrahydrofuran; for 2h; Heating / reflux;	84%
With Lawessons reagent; In tetrahydrofuran; for 2h; Reflux;	65%
With Lawessons reagent; In tetrahydrofuran; for 6h; Heating;	53%
With tetraphosphorus decasulfide; Hexamethyldisiloxane; In toluene; at 45 ℃; for 15h;	44%
With P₂S₂; In benzene; for 96h; Heating;
With Lawessons reagent;
With Lawessons reagent; In tetrahydrofuran; for 18h; Heating / reflux;
With Lawessons reagent; In tetrahydrofuran; for 6h; Reflux;