What is the 3,5-Di(trifluoromethyl)benzamide?

3,5-Di(trifluoromethyl)benzamide is WHITE TO TAN POWDER, CRYSTALS POWDER AND/OR CHUNKS, while it's Molecular Formula is C9H5F6NO. WHITE TO TAN POWDER, CRYSTALS POWDER AND/OR CHUNKS Used in Organic Synthesis: 3,5-Di(trifluoromethyl)benzamide is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic molecules. Its unique structure and properties make it a valuable component in the creation of new compounds with potential applications in various fields. Used in Drug Discovery Research: In the pharmaceutical industry, 3,5-Di(trifluoromethyl)benzamide is utilized as a key intermediate in drug discovery research. Its presence in the molecular structure can influence the pharmacological properties of the resulting compounds, potentially leading to the development of new therapeutic agents. Used in the Synthesis of Agrochemicals: 3,5-Di(trifluoromethyl)benzamide is employed as a starting material in the synthesis of agrochemicals, where its chemical properties can enhance the effectiveness of pesticides, herbicides, and other agricultural products. Used in the Development of Fluorine-Containing Materials: 3,5-Di(trifluoromethyl)benzamide is also used in the development of fluorine-containing materials, which have a wide range of industrial applications. The introduction of fluorine atoms can significantly alter the physical and chemical properties of materials, making them suitable for use in various high-performance applications, such as in the electronics, automotive, and aerospace industries.

What is the CAS number for 3,5-Di(trifluoromethyl)benzamide?

The CAS number of 3,5-Di(trifluoromethyl)benzamide is 22227-26-5.

What is 3,5-Di(trifluoromethyl)benzamide (22227-26-5) used for?

3,5-Di(trifluoromethyl)benzamide is a chemical compound characterized by the molecular formula C9H6F6NO. It is a white solid that features two trifluoromethyl groups attached to a benzene ring and an amide functional group. Known for its high thermal stability, 3,5-Di(trifluoromethyl)benzamide serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, as well as in the development of fluorine-containing materials for diverse industrial applications.InChI:InChI=1/C9H5F6NO/c10-8(11,12)5-1-4(7(16)17)2-6(3-5)9(13,14)15/h1-3H,(H2,16,17)

What is the 3,5-Di(trifluoromethyl)benzamide?

3,5-Di(trifluoromethyl)benzamide is WHITE TO TAN POWDER, CRYSTALS POWDER AND/OR CHUNKS, while it's Molecular Formula is C9H5F6NO. WHITE TO TAN POWDER, CRYSTALS POWDER AND/OR CHUNKS Used in Organic Synthesis: 3,5-Di(trifluoromethyl)benzamide is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic molecules. Its unique structure and properties make it a valuable component in the creation of new compounds with potential applications in various fields. Used in Drug Discovery Research: In the pharmaceutical industry, 3,5-Di(trifluoromethyl)benzamide is utilized as a key intermediate in drug discovery research. Its presence in the molecular structure can influence the pharmacological properties of the resulting compounds, potentially leading to the development of new therapeutic agents. Used in the Synthesis of Agrochemicals: 3,5-Di(trifluoromethyl)benzamide is employed as a starting material in the synthesis of agrochemicals, where its chemical properties can enhance the effectiveness of pesticides, herbicides, and other agricultural products. Used in the Development of Fluorine-Containing Materials: 3,5-Di(trifluoromethyl)benzamide is also used in the development of fluorine-containing materials, which have a wide range of industrial applications. The introduction of fluorine atoms can significantly alter the physical and chemical properties of materials, making them suitable for use in various high-performance applications, such as in the electronics, automotive, and aerospace industries.

What is the CAS number for 3,5-Di(trifluoromethyl)benzamide?

The CAS number of 3,5-Di(trifluoromethyl)benzamide is 22227-26-5.

What is 3,5-Di(trifluoromethyl)benzamide (22227-26-5) used for?

3,5-Di(trifluoromethyl)benzamide is a chemical compound characterized by the molecular formula C9H6F6NO. It is a white solid that features two trifluoromethyl groups attached to a benzene ring and an amide functional group. Known for its high thermal stability, 3,5-Di(trifluoromethyl)benzamide serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals, as well as in the development of fluorine-containing materials for diverse industrial applications.InChI:InChI=1/C9H5F6NO/c10-8(11,12)5-1-4(7(16)17)2-6(3-5)9(13,14)15/h1-3H,(H2,16,17)

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Product classification

3,5-Di(trifluoromethyl)benzamide

Name: 3,5-Di(trifluoromethyl)benzamide
CAS: 22227-26-5
Purity: 99%

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Details

Factory supply 3,5-Di(trifluoromethyl)benzamide 22227-26-5 with sufficient production capacity

Molecular Formula: C9H5F6NO
Molecular Weight: 257.135
Appearance/Colour: WHITE TO TAN POWDER, CRYSTALS POWDER AND/OR CHUNKS
Vapor Pressure: 0.468mmHg at 25°C
Melting Point: 163-167 °C(lit.)
Refractive Index: 1.428
Boiling Point: 193.3 °C at 760 mmHg
PKA: 14.62±0.50(Predicted)
Flash Point: 70.7 °C
PSA： 43.09000
Density: 1.468 g/cm³
LogP: 3.52340

3,5-Di(trifluoromethyl)benzamide(Cas 22227-26-5) Usage

General Description

3,5-Di(trifluoromethyl)benzamide is a chemical compound with the molecular formula C9H6F6NO. It is a white solid that is used in organic synthesis and drug discovery research. 3,5-Di(trifluoromethyl)benzamide has two trifluoromethyl groups attached to a benzene ring, and an amide functional group. 3,5-Di(trifluoromethyl)benzamide is known to have high thermal stability and is used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used in the development of fluorine-containing materials with various industrial applications.

InChI:InChI=1/C9H5F6NO/c10-8(11,12)5-1-4(7(16)17)2-6(3-5)9(13,14)15/h1-3H,(H2,16,17)

22227-26-5 Relevant articles

Azole derivative or pharmaceutically acceptable salt thereof as well as preparation method and application of azole derivative or pharmaceutically acceptable salt thereof

-

Paragraph 0038-0043, (2021/03/24)

The invention discloses an azole derivat...

Hydrosilylative reduction of primary amides to primary amines catalyzed by a terminal [Ni-OH] complex

Bera, Jitendra K.,Pandey, Pragati

supporting information, p. 9204 - 9207 (2021/09/20)

A terminal [Ni-OH] complex1, supported b...

Identifying Amidyl Radicals for Intermolecular C-H Functionalizations

Tierney, Matthew M.,Crespi, Stefano,Ravelli, Davide,Alexanian, Erik J.

, p. 12983 - 12991 (2019/10/02)

Recent studies have demonstrated the cap...

Synthetic process of Selinexor intermediate

-

Paragraph 0053-0061, (2017/08/29)

The invention provides a synthetic proce...

22227-26-5 Process route

: 401-96-7
3,5-bis(trifluoromethyl)benzoyl fluoride

: 22227-26-5
3,5-Bis(trifluoromethyl)benzamide

Conditions

Conditions	Yield
With ammonia; In water; toluene; at 30 ℃; for 6h;	95%

: 27126-93-8
3,5-bis(trifluoromethyl)benzonitrile

: 22227-26-5
3,5-Bis(trifluoromethyl)benzamide

Conditions

Conditions	Yield
3,5-bis(trifluoromethyl)benzonitrile; With sodium hydroxide; In N,N-dimethyl-formamide; at 15 ℃; for 0.333333h; Autoclave; Large scale; With magnesium(II) chloride hexahydrate; In N,N-dimethyl-formamide; at 10 - 20 ℃; for 4h; Autoclave; Large scale;	1931 g
With sodium hydrogen sulfide; magnesium chloride; In N,N-dimethyl-formamide; at 20 ℃; for 3h;

22227-26-5 Upstream products

328-70-1
3,6-bis(trifluoromethyl)bromobenzene
401-96-7
3,5-bis(trifluoromethyl)benzoyl fluoride
110-54-3
hexane
7688-25-7
1,4-di(diphenylphosphino)-butane

22227-26-5 Downstream products

67048-86-6
5-(3,5-bis-trifluoromethyl-phenyl)-[1,3,4]oxathiazol-2-one
67048-81-1
3-(3,5-bis-trifluoromethyl-phenyl)-isothiazole-4-carboxylic acid
67049-18-7
3-(3,5-bis-trifluoromethyl-phenyl)-isothiazole-4-carboxylic acid ethyl ester
67048-64-0
3-(3,5-bis-trifluoromethyl-phenyl)-isothiazole-4,5-dicarboxylic acid

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