Description
Valerophenone (CAS 1009-14-9) is also known as 1-phenyl-1 pentanone or Butyl Phenyl Ketone. It is a colorless liquid with a pleasant floral smell that is usually made by acylating benzene with valeryl chloride. Being prochiral, valerophenone undergoes enantioselective hydrogenation to the corresponding alcohol.
Valerophenone CAS 1009-14-9 Technical Information
Name | Valerophenone |
Cas No. | 1009-14-9 |
Formula | C11H14O |
Synonyms | MFCD00009480;Pentanophenone;Butyl Phenyl Ketone;EINECS 213-767-3;Valerophenone;1-Phenylpentan-1-one |
Molecular weight | 162.23 |
Color | colorless |
Appearance | colorless liquid |
Valerophenone Markets/Application:
Valerophenone is used across diverse industries, with applications including:
Fragrances and flavors: Valerophenone, CAS 1009-14-9, plays an integral part in producing fragrances and flavors. Its sweet floral fragrance enhances perfumes, cosmetics, and food products with enhanced sensory appeal.
Chemical Synthesis: Organic synthesis relies heavily on valerophenone for the production of various products, including pharmaceuticals, agrochemicals, and specialty polymers. Valerophenone serves a crucial role as an intermediary in this production chain.
Pharmaceuticals: Valerophenone (CAS 1009-14-9) is extensively used in pharmaceutical manufacturing for synthesizing specific drug intermediates that advance medical science.
Research and Development: Valerophenone, used as an innovative reagent in chemical experiments and reactions, can support research laboratories in supporting innovation within chemistry.
Photochemistry: Valerophenone serves as a photoinitiator, facilitating light-induced reactions. These reactions encompass photochemical polymerization, photocrosslinking, and other light-driven organic synthesis processes. Furthermore, valerophenone is employed as a precursor for photosensitive dyes, especially in dye-sensitized solar cells and other optoelectronic devices.
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Reference: Wikipedia-Valerophenone, PubChem-Valerophenone
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