What is the 4-Fluorobenzanilide?

4-Fluorobenzanilide is , while it's Molecular Formula is C13H10FNO. Used in Pharmaceutical Industry: 4-Fluorobenzanilide is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of a wide range of organic compounds with potential medicinal properties. Used in Organic Synthesis: In the field of organic synthesis, 4-Fluorobenzanilide serves as a key building block for the assembly of more complex molecules. Its reactivity and structural features make it a valuable component in the synthesis of various organic compounds. Used in Medicinal Chemistry: 4-Fluorobenzanilide has been studied for its potential applications in medicinal chemistry, where it may contribute to the discovery of new drugs and therapeutic agents. Its unique structure and properties make it a promising candidate for further research and development. Used in Pharmacological Research: 4-Fluorobenzanilide has been investigated for its potential pharmacological properties, including its role as a potential analgesic or anti-inflammatory agent. This research aims to explore the compound's therapeutic potential and its ability to alleviate pain or reduce inflammation in various conditions.

What is the CAS number for 4-Fluorobenzanilide?

The CAS number of 4-Fluorobenzanilide is 366-63-2.

What is 4-Fluorobenzanilide (366-63-2) used for?

4-Fluorobenzanilide is an organic compound with the chemical formula C13H10FNO2. It is a derivative of benzanilide, featuring a fluorine atom at the 4-position on the benzene ring. This white crystalline solid is primarily used as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its molecular structure consists of a benzene ring with a fluorine atom, an amide group, and an aniline group attached to it. 4-Fluorobenzanilide is known for its reactivity and can participate in various chemical reactions, such as nucleophilic aromatic substitution, making it a valuable building block in the development of new compounds with potential applications in various industries.InChI:InChI=1/C13H10FNO/c14-11-8-6-10(7-9-11)13(16)15-12-4-2-1-3-5-12/h1-9H,(H,15,16)

What is the 4-Fluorobenzanilide?

4-Fluorobenzanilide is , while it's Molecular Formula is C13H10FNO. Used in Pharmaceutical Industry: 4-Fluorobenzanilide is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of a wide range of organic compounds with potential medicinal properties. Used in Organic Synthesis: In the field of organic synthesis, 4-Fluorobenzanilide serves as a key building block for the assembly of more complex molecules. Its reactivity and structural features make it a valuable component in the synthesis of various organic compounds. Used in Medicinal Chemistry: 4-Fluorobenzanilide has been studied for its potential applications in medicinal chemistry, where it may contribute to the discovery of new drugs and therapeutic agents. Its unique structure and properties make it a promising candidate for further research and development. Used in Pharmacological Research: 4-Fluorobenzanilide has been investigated for its potential pharmacological properties, including its role as a potential analgesic or anti-inflammatory agent. This research aims to explore the compound's therapeutic potential and its ability to alleviate pain or reduce inflammation in various conditions.

What is the CAS number for 4-Fluorobenzanilide?

The CAS number of 4-Fluorobenzanilide is 366-63-2.

What is 4-Fluorobenzanilide (366-63-2) used for?

4-Fluorobenzanilide is an organic compound with the chemical formula C13H10FNO2. It is a derivative of benzanilide, featuring a fluorine atom at the 4-position on the benzene ring. This white crystalline solid is primarily used as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its molecular structure consists of a benzene ring with a fluorine atom, an amide group, and an aniline group attached to it. 4-Fluorobenzanilide is known for its reactivity and can participate in various chemical reactions, such as nucleophilic aromatic substitution, making it a valuable building block in the development of new compounds with potential applications in various industries.InChI:InChI=1/C13H10FNO/c14-11-8-6-10(7-9-11)13(16)15-12-4-2-1-3-5-12/h1-9H,(H,15,16)

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Chemical Name 4-Fluorobenzanilide
CAS No. 366-63-2
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Factory Supply industrial standard 4-Fluorobenzanilide 366-63-2 In Stock

Molecular Formula: C13H10FNO
Molecular Weight: 215.227
Vapor Pressure: 0.014mmHg at 25°C
Melting Point: 182-184 °C
Boiling Point: 258.1°Cat760mmHg
PKA: 13.39±0.70(Predicted)
Flash Point: 109.9°C
PSA： 29.10000
Density: 1.247g/cm³
LogP: 3.15100

4-Fluorobenzanilide(Cas 366-63-2) Usage

General Description

4-Fluorobenzanilide, also known as 4-fluoro-N-phenylbenzamide, is an organic compound that consists of a fluorine atom attached to a benzene ring, and an amide group bonded to the phenyl ring. It is a white solid that is sparingly soluble in water but dissolves in organic solvents. 4-Fluorobenzanilide is commonly used as an intermediate in the production of pharmaceuticals and other organic compounds. It has also been studied for its potential use in organic synthesis and medicinal chemistry applications. Additionally, it has been investigated for its potential pharmacological properties, including its role as a potential analgesic or anti-inflammatory agent.

InChI:InChI=1/C13H10FNO/c14-11-8-6-10(7-9-11)13(16)15-12-4-2-1-3-5-12/h1-9H,(H,15,16)

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366-63-2 Process route

: 347-84-2
1-(4-fluorophenyl)-2-phenylethanone

: 62-53-3
aniline

: 366-63-2
4-fluoro-N-phenylbenzamide

: 100-52-7
benzaldehyde

Conditions

Conditions	Yield
With 1,10-Phenanthroline; copper(II) chloride dihydrate; oxygen; In acetonitrile; for 36h; under 760.051 Torr; Reflux;	67% 98 %Chromat.

: 459-57-4
4-fluorobenzaldehyde

: 62-53-3
aniline

: 366-63-2
4-fluoro-N-phenylbenzamide

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel ⁽⁰⁾; 2,2,2-Trifluoroacetophenone; 1,3-bis-(2,6-diisopropylphenyl)-imidazol-2-ylidene; In 1,4-dioxane; at 40 ℃; for 8h; Inert atmosphere; Glovebox;	97%
aniline; With C₁₂H₃₀NaO₆⁽¹⁺⁾*C₅₆H₈₄O₄Sm^(1-); In tetrahydrofuran; for 0.5h; Inert atmosphere; 4-fluorobenzaldehyde; In tetrahydrofuran; at 25 ℃; for 3h; Inert atmosphere;	82%
aniline; With C₂₄H₄₈KO₆⁽¹⁺⁾*C₁₀₈H₁₅₂KLa₂O₁₂^(1-); for 0.5h; Inert atmosphere; 4-fluorobenzaldehyde; at 25 ℃; for 22h; Inert atmosphere;	79%
aniline; With C₅₆H₈₆F₂Li₂N₃O₄Si₂Sm; In tetrahydrofuran; at 25 ℃; for 0.5h; Inert atmosphere; Glovebox; 4-fluorobenzaldehyde; In tetrahydrofuran; at 25 ℃; for 3h; Inert atmosphere; Glovebox;	74%
With tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide; In acetonitrile; at 80 ℃; for 6h;	71%
aniline; With C₅₈H₉₂La₂N₆O₄Si₄; In tetrahydrofuran; at 20 ℃; for 0.5h; Inert atmosphere; 4-fluorobenzaldehyde; In tetrahydrofuran; for 3h; Inert atmosphere;	71%
4-fluorobenzaldehyde; With potassium carbonate; In neat (no solvent); at 85 ℃; for 0.333333h; aniline; In neat (no solvent); at 85 ℃;	43%