What is the 4-FLUOROBENZALDEHYDE OXIME?

4-FLUOROBENZALDEHYDE OXIME is , while it's Molecular Formula is C7H6FNO. Used in Organic Synthesis: 4-Fluorobenzaldehyde oxime is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules. Used in Pharmaceutical Production: In the pharmaceutical industry, 4-Fluorobenzaldehyde oxime is utilized as a building block in the synthesis of a range of drugs, leveraging its chemical properties to create effective medicinal compounds. Used in Agrochemical Production: Similarly, in the agrochemical sector, 4-Fluorobenzaldehyde oxime serves as a key intermediate in the development of various agrochemicals, enhancing crop protection and yield. Used in Dye and Perfume Synthesis: 4-Fluorobenzaldehyde oxime is employed as an intermediate in the synthesis of dyes and perfumes, where its chemical structure contributes to the color and fragrance of these products. Used in Medicinal Chemistry: In the field of medicinal chemistry, 4-Fluorobenzaldehyde oxime shows potential as an inhibitor for certain enzymes and receptors, playing a role in the development of new therapeutic agents. Used in Metal Extraction Processes: As a chelating agent, 4-Fluorobenzaldehyde oxime is used in metal extraction processes, where its ability to form stable complexes with metal ions aids in their separation and purification. Used in Analytical Chemistry: In analytical chemistry, 4-Fluorobenzaldehyde oxime functions as a reagent, assisting in the identification, measurement, and analysis of various chemical substances.

What is the CAS number for 4-FLUOROBENZALDEHYDE OXIME?

The CAS number of 4-FLUOROBENZALDEHYDE OXIME is 588-95-4.

What is 4-FLUOROBENZALDEHYDE OXIME (588-95-4) used for?

4-Fluorobenzaldehyde oxime is a chemical compound derived from fluorobenzaldehyde and hydroxylamine. It is characterized by its reactivity and versatility, making it a valuable reagent in organic synthesis and a key building block in the production of pharmaceuticals and agrochemicals. Its unique properties also extend its applications to various fields, including the synthesis of dyes, perfumes, and other organic compounds, as well as its potential use in medicinal chemistry for enzyme and receptor inhibition.InChI:InChI=1/C7H6FNO/c8-7-3-1-6(2-4-7)5-9-10/h1-5,10H/b9-5+

What is the 4-FLUOROBENZALDEHYDE OXIME?

4-FLUOROBENZALDEHYDE OXIME is , while it's Molecular Formula is C7H6FNO. Used in Organic Synthesis: 4-Fluorobenzaldehyde oxime is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules. Used in Pharmaceutical Production: In the pharmaceutical industry, 4-Fluorobenzaldehyde oxime is utilized as a building block in the synthesis of a range of drugs, leveraging its chemical properties to create effective medicinal compounds. Used in Agrochemical Production: Similarly, in the agrochemical sector, 4-Fluorobenzaldehyde oxime serves as a key intermediate in the development of various agrochemicals, enhancing crop protection and yield. Used in Dye and Perfume Synthesis: 4-Fluorobenzaldehyde oxime is employed as an intermediate in the synthesis of dyes and perfumes, where its chemical structure contributes to the color and fragrance of these products. Used in Medicinal Chemistry: In the field of medicinal chemistry, 4-Fluorobenzaldehyde oxime shows potential as an inhibitor for certain enzymes and receptors, playing a role in the development of new therapeutic agents. Used in Metal Extraction Processes: As a chelating agent, 4-Fluorobenzaldehyde oxime is used in metal extraction processes, where its ability to form stable complexes with metal ions aids in their separation and purification. Used in Analytical Chemistry: In analytical chemistry, 4-Fluorobenzaldehyde oxime functions as a reagent, assisting in the identification, measurement, and analysis of various chemical substances.

What is the CAS number for 4-FLUOROBENZALDEHYDE OXIME?

The CAS number of 4-FLUOROBENZALDEHYDE OXIME is 588-95-4.

What is 4-FLUOROBENZALDEHYDE OXIME (588-95-4) used for?

4-Fluorobenzaldehyde oxime is a chemical compound derived from fluorobenzaldehyde and hydroxylamine. It is characterized by its reactivity and versatility, making it a valuable reagent in organic synthesis and a key building block in the production of pharmaceuticals and agrochemicals. Its unique properties also extend its applications to various fields, including the synthesis of dyes, perfumes, and other organic compounds, as well as its potential use in medicinal chemistry for enzyme and receptor inhibition.InChI:InChI=1/C7H6FNO/c8-7-3-1-6(2-4-7)5-9-10/h1-5,10H/b9-5+

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4-FLUOROBENZALDEHYDE OXIME

CAS：588-95-4
purity：99%

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Molecular Formula: C7H6FNO
Molecular Weight: 139.129
Melting Point: 82-85 °C (lit.)
Boiling Point: 194.9 °C at 760 mmHg
PKA: 11.18±0.10(Predicted)
Flash Point: 71.7 °C
PSA： 32.59000
Density: 1.14 g/cm³
LogP: 1.63380

4-FLUOROBENZALDEHYDE OXIME(Cas 588-95-4) Usage

General Description

4-Fluorobenzaldehyde oxime is a chemical compound that is derived from fluorobenzaldehyde and hydroxylamine. It is commonly used as a reagent in organic synthesis and as a building block in the production of various pharmaceuticals and agrochemicals. 4-FLUOROBENZALDEHYDE OXIME has a wide range of applications, including as an intermediate in the synthesis of dyes, perfumes, and other organic compounds. It also exhibits potential for use in medicinal chemistry, particularly in the development of inhibitors for certain enzymes and receptors. Additionally, its properties make it suitable for use as a chelating agent in metal extraction processes and as a reagent in analytical chemistry. Overall, 4-Fluorobenzaldehyde oxime is a versatile compound with diverse uses in both the industrial and research sectors.

InChI:InChI=1/C7H6FNO/c8-7-3-1-6(2-4-7)5-9-10/h1-5,10H/b9-5+

588-95-4 Relevant articles

Visible-light mediated stereospecific C(sp2)-H difluoroalkylation of (Z)-aldoximes

Chen, Hua,Deng, Hongmei,Gong, Haiying,Hao, Jian,Li, Mingjie,Peng, Yi,Wan, Wen,Wang, Qian,Zhang, Yifang

supporting information, p. 7867 - 7874 (2021/09/28)

A visible light mediated stereospecific ...

Water mediated procedure for preparation of stereoselective oximes as inhibitors of MRCK kinase

Luqman, Suaib,Misra, Krishna,Pandey, Jyoti,Shrivash, Manoj Kumar,Shukla, Akhilesh Kumar,Singh, Shilipi

, (2020/07/08)

Stereoselective aldoximes, preferably Z ...

ISOXAZOLO-PYRIDAZINE DERIVATIVES

-

, (2009/06/27)

The invention relates to isoxazolo-pyrid...

(E)-Phenyl- and -heteroaryl-substituted O-benzoyl-(or acyl)oximes as lipoprotein-associated phospholipase A2 inhibitors

Jeong, Tae-Sook,Kim, Mi Jeong,Yu, Hana,Kim, Kyung Soon,Choi, Joong-Kwon,Kim, Sung-Soo,Lee, Woo Song

, p. 1525 - 1527 (2007/10/03)

A series of (E)-phenyl- and -heteroaryl-...

588-95-4 Process route

: 18861-57-9,50737-52-5
ethyl (E)-2-cyano-3-(4-fluorophenyl)-2-propenoate

: 588-95-4,7304-35-0
syn-4-fluorobenzaldoxime

Conditions

Conditions	Yield
With hydroxylamine hydrochloride; sodium carbonate; In methanol; water; at 100 ℃; for 1h; stereoselective reaction;	92%

: 459-57-4
4-fluorobenzaldehyde

: 588-95-4,7304-35-0
syn-4-fluorobenzaldoxime