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CAS 403-42-9

4'-Fluoroacetophenone TCI F0261

4'-Fluoroacetophenone TCI F0261

Chemical Identity

CAS No.
403-42-9
PubChem
CID 9828·SID 87570038
Formula
C8H7FO
Molecular weight
138.14 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-(4-fluorophenyl)ethanone
SMILES
CC(=O)C1=CC=C(C=C1)F
InChIKey
ZDPAWHACYDRYIW-UHFFFAOYSA-N
MDL
MDL00000354
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4'-Fluoroacetophenone is a chemical compound widely used in organic reactions, particularly in the synthesis of fluorinated compounds. It serves as a key building block in the development of pharmaceuticals, industrial chemicals, and research materials. This compound features a fluoro group at the para position (4') and a ketone group on the phenyl chain, making it highly versatile in synthetic chemistry. Its presence in laboratory settings enables the creation of complex molecules through various reaction mechanisms.

The unique properties of 4'-Fluoroacetophenone make it a preferred choice in chemical synthesis. The fluoro group introduces polarity and reactivity, influencing the stability and behavior of the compound during reactions. Its solubility in organic solvents like ethyl acetate and ethanol enhances its usability in diverse chemical processes. These characteristics allow it to be a reliable reagent in both academic and industrial research environments.

In Indonesian laboratories, 4'-Fluoroacetophenone is commonly used in organic synthesis, drug development, and chemical research. Its reactivity and structural versatility make it an essential component for scientists working on fluorinated compounds. It is frequently employed in substitution reactions, Friedel-Crafts reactions, and nucleophilic reactions, supporting a wide range of experimental applications.

TCI brochures (PDF)

  • Organic synthesis: 4'-Fluoroacetophenone is ideal for creating fluorinated compounds due to its reactivity and structural versatility.
  • Pharmaceutical research: It is used in the development of new drugs because of its ability to participate in complex molecular transformations.
  • Industrial chemical production: Its stability and solubility make it suitable for large-scale chemical manufacturing processes.
  • Nucleophilic substitution reactions: The fluoro group enhances its utility in reactions where nucleophilic attack is required.
  • Research and development: It is a valuable reagent for scientists exploring new chemical pathways and molecular structures.

Brand TCI
CAS number 403-42-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid or liquid depending on the specific product variant
Storage Store in a cool, dry place away from direct sunlight

4'-Fluoroacetophenone should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong bases or reducing agents. Proper labeling and storage conditions help ensure safety and maintain the quality of the compound during laboratory use.

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