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CAS 459-23-4

4-Fluorobenzaldehyde Oxime TCI F1367

4-Fluorobenzaldehyde Oxime TCI F1367

Chemical Identity

Other names
4-Fluorobenzaldoxime · p-Fluorobenzaldehyde Oxime
CAS No.
459-23-4
PubChem
CID 5372466
Formula
C7H6FNO
Molecular weight
139.13 g/mol
Purity
>95.0%(HPLC)
Storage
0-10°C
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(NZ)-N-[(4-fluorophenyl)methylidene]hydroxylamine
SMILES
C1=CC(=CC=C1C=NO)F
InChIKey
FSKSLWXDUJVTHE-UITAMQMPSA-N
MDL
MDL00133101
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4-Fluorobenzaldehyde Oxime is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a versatile building block in laboratory settings, enabling the creation of compounds with specific structural features. Its unique combination of a fluorine group and an oxime functional group provides both reactivity and selectivity in chemical transformations. This compound is particularly valuable in synthetic chemistry due to its ability to participate in a variety of reaction mechanisms, including nucleophilic and condensation reactions.

The compound's stability and high reactivity make it a preferred choice for researchers working on organic synthesis. The presence of the fluorine atom contributes to its chemical stability, while the oxime group enhances its reactivity in various synthetic pathways. These properties allow it to be a reliable component in both academic and industrial research environments. Its ability to undergo substitution reactions and other chemical transformations makes it a key reagent in the development of new materials and pharmaceutical compounds.

In Indonesian laboratories, 4-Fluorobenzaldehyde Oxime is commonly used in organic chemistry research, especially in the fields of pharmacy and material science. Its availability and competitive pricing make it a popular choice for researchers needing a reactive and specific building block. Its role in the synthesis of complex organic compounds is well recognized, making it an essential reagent for many experimental applications.

  • Organic synthesis of fluorinated compounds due to its stable fluorine group and reactive oxime functionality.
  • Development of pharmaceutical intermediates where controlled reactivity and structural specificity are required.
  • Creation of advanced materials through chemical modifications that benefit from fluorinated building blocks.
  • Research in nucleophilic and condensation reactions where the oxime group enhances reaction efficiency.
  • Investigation of reaction mechanisms involving fluorinated aromatic systems for academic and industrial purposes.

Brand TCI
CAS number 459-23-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

4-Fluorobenzaldehyde Oxime should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene. Due to its reactivity, it should be handled with care, and appropriate personal protective equipment should be worn when working with it. The compound is best kept in a well-ventilated area to minimize exposure to vapors. Regular monitoring of storage conditions is advised to ensure the compound remains stable and suitable for use in laboratory applications.

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