2'-Fluoro-4'-hydroxyacetophenone TCI F0418

Chemical Identity

CAS No.: 98619-07-9
PubChem: CID 2724912·SID 87570185
Formula: C8H7FO2
Molecular weight: 154.14 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-(2-fluoro-4-hydroxyphenyl)ethanone
SMILES: CC(=O)C1=C(C=C(C=C1)O)F
InChIKey: ZCZIRBNZMFUCOH-UHFFFAOYSA-N
MDL: MDL00142713

Rp 530.250,00

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Berat 1g 5g

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2'-Fluoro-4'-hydroxyacetophenone is a chemical compound widely used as a building block in the synthesis of complex molecules. It plays a crucial role in organic chemistry laboratories, where it serves as a versatile intermediate for various synthetic pathways. This compound is particularly valuable for its ability to undergo substitution reactions involving fluorine and hydroxyl groups, making it an essential tool for chemists working on functional group modifications. Its presence in laboratory settings is vital for the development of new compounds with tailored properties.

The compound's chemical stability and reactivity make it a preferred choice for researchers. Its fluorine and hydroxyl substituents contribute to unique reactivity profiles, enabling participation in both nucleophilic and electrophilic reactions. These properties allow it to be a key player in the synthesis of pharmaceuticals and advanced materials. The combination of stability and reactivity ensures that it remains a reliable and effective reagent in a wide range of chemical processes.

In Indonesian laboratories, 2'-Fluoro-4'-hydroxyacetophenone is commonly used in research related to organic chemistry, pharmaceutical development, and material science. Its high reactivity and structural versatility make it a go-to compound for researchers aiming to create new compounds with medical or industrial applications. Its role in both academic and industrial research underscores its importance in the chemical sciences.

TCI brochures (PDF)

Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 22

Related TCI products

Synthesis of pharmacological compounds requiring fluorine substitution on phenyl structures, as it provides a stable and reactive platform for further modifications.
Development of innovative materials through functional group manipulation, where its hydroxyl and fluorine groups enable tailored molecular properties.
Organic chemistry research involving nucleophilic and electrophilic reactions, due to its ability to participate in a wide range of chemical transformations.
Pharmaceutical compound design where structural modifications are needed to enhance bioavailability or therapeutic effects.
Chemical synthesis projects requiring versatile intermediates that can be easily modified through various reaction mechanisms.

Brand	TCI
CAS number	98619-07-9
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 formulation
Storage	Store in a cool, dry place away from direct sunlight and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it should be stored separately from strong oxidizers and incompatible substances to ensure safety. Regular monitoring of storage conditions is advised to maintain the integrity of the compound during long-term use.

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