28593-14-8 Usage
Uses
Used in Organic Synthesis:
4-Fluoropentylbenzene is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for the formation of new chemical bonds and the synthesis of complex molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-fluoropentylbenzene is utilized as an intermediate in the synthesis of various drugs. Its presence in the molecular structure of these drugs can contribute to their therapeutic properties and effectiveness.
Used in Agrochemical Production:
4-Fluoropentylbenzene is also employed in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their efficacy in controlling pests and weeds in agricultural settings.
Used in Dye Manufacturing:
In the dye industry, 4-fluoropentylbenzene is used as a starting material for the synthesis of various dyes. Its unique chemical properties enable the creation of dyes with specific color characteristics and stability.
Used in Resin and Plastic Production:
4-Fluoropentylbenzene is utilized in the manufacturing of resins and plastics, where it contributes to the physical and chemical properties of these materials. Its presence in resins and plastics can improve their durability, flexibility, and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 28593-14-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,9 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28593-14:
(7*2)+(6*8)+(5*5)+(4*9)+(3*3)+(2*1)+(1*4)=138
138 % 10 = 8
So 28593-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H15F/c1-2-3-4-5-10-6-8-11(12)9-7-10/h6-9H,2-5H2,1H3
28593-14-8Relevant academic research and scientific papers
Catechol diethers as selective PDE IV inhibitors
-
, (2008/06/13)
This invention relates to 4-substituted catechol diether compounds which are selective inhibitors of phosphodiesterase (PDE) type IV. The compounds of the present invention are useful in inhibiting PDE IV and in the treatment of AIDS, asthma, bronchitis, chronic obstructive airways disease, psoriasis, allergic rhinitis, dermatitis and other inflammatory diseases. This invention also relates to pharmaceutical compositions comprising the compounds hereof
Structure of ω-Arylalkyl Radicals: A 13C CIDNP Investigation
Olah, George A.,Krishnamurthy, V. V.,Singh, Brij P.,Iyer, Pradeep S.
, p. 955 - 963 (2007/10/02)
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.
