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Valerophenone CAS 1009-14-9

CAS Number: 1009-14-9
Chemical Name: Valerophenone, Butyl Phenyl Ketone, 1 phenyl 1 pentanone
Molecular Formula: C11H14O
PubChem CID: 66093
Appearance: Colorless liquid
Solubility: Soluble in organic solvents
Molecular Weight: 162.23 g/mol
Application: Fragrances and flavors, chemical synthesis, photochemistry

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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