28593-12-6

Usage

Uses

Used in Pharmaceutical Industry:
1-Fluoro-3-propylbenzene is used as an intermediate in the synthesis of various pharmaceutical compounds for its versatile chemical properties and reactivity.
Used in Agrochemical Industry:
1-Fluoro-3-propylbenzene is used as a precursor in the development of agrochemicals, contributing to the production of effective pesticides and other agricultural products.
Used in Dye Industry:
1-Fluoro-3-propylbenzene is utilized in the creation of dyes, taking advantage of its chemical structure to produce a range of colorants for various applications.
Used in Laboratory Settings:
1-Fluoro-3-propylbenzene is used as a solvent for organic reactions, providing a suitable medium for various chemical processes and experiments. Its use in laboratories is attributed to its ability to dissolve a wide range of organic compounds and facilitate desired reactions.

Upstream product

• 38340-11-3 1-fluoro-3-(1-propen-1-yl)benzene 
• 701-38-2 1-(3-fluorophenyl)propan-1-ol 
• 1073-06-9 3-fluorobromobenzene 
• 30984-53-3 1-allyl-3-fluorobenzene 
• 84680-82-0 C₁₇H₁₄ClFO₄ 
• 84648-67-9 C₁₂H₁₃FO₄ 

Downstream Products

• 1345025-44-6 1-(3,4-difluorophenyl)-4-(2-fluoro-4-propylphenyl)bicyclo[2.2.2]octane 
• 321939-65-5 2-fluoro-1-iodo-4-propylbenzene 
• 442661-38-3 4-n-propyl-2-fluorophenylboronic acid 
• 172748-78-6 (R)-1-(3-fluoro-phenyl)-propan-1-ol 
• 172748-78-6 (S)-1-(3'-fluorophenyl)propan-1-ol 

Relevant academic research and scientific papers

Synthesis and mesomorphic properties of laterally fluorinated alkyl 4′′-alkylterphenyl-4-yl carbonate liquid crystals

Fifteen series of homologues of a variety of mono-, di- and trifluorosubstituted alkyl 4′′-alkylterphenyl-4-yl carbonates have been synthesized and their mesomorphic properties have been determined. From among 95 prepared compounds, 40 pure nematogens have been found, as well as 55 mesogens with orthogonal and tilted smectic phases in broad temperature ranges. The type and combination of the LC phase strongly depend on the position and number of the fluorine atoms. Physical properties and correlations between the molecular core fluorosubstitution, the length of the terminal chains and the type and sequence of the liquid crystalline phases, have been determined. The compounds are useful for the formulation of nematic mixtures as well as ferroelectric ones.

Liquid crystal carbonate and liquid crystal medium containing the same with positive or negative dielectric anisotropy

A novel liquid crystalline carbonate and the mixture containing the same: wherein R3 is an alkyl (H2n+1Cn) or an alkenyl (H2n?1Cn) group, each of 1 to 12 carbon atoms, the ring A is laterally unsubstituted benze

New fluorine substituted liquid crystal containing bicyclo[2.2.2]octane unit

We have designed and synthesized a new series of liquid crystalline compounds with hybridized three-ring system based on bicyclo[2.2.2]octane unit together with fluorine substituted phenyl and biphenyl fragments. The key stages of the synthesis are alkyla

Structure of ω-Arylalkyl Radicals: A 13C CIDNP Investigation

Thermolysis of a series of ω-arylalkanoyl m-chlorobenzoyl (and acetyl) peroxides at ca. 100 deg C in cyclohexanone and in hexachloroacetone was studied by using 13C chemically induced dynamic nuclear polarization.Analysis of the observed 13C polarizations indicate that all the three radicals (β-arylethyl, γ-arylpropyl and δ-arylbutyl) have open-chain structures with no evidence for aryl participation resulting in spirocycloalkylcyclohexadienyl radicals.