108976-70-1

Basic information

• Product Name: 2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE
• Synonyms: 2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE
• CAS NO: 108976-70-1
• Molecular Formula: C₁₇H₁₈O
• Molecular Weight: 238.32
• Mol File: 108976-70-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 387.4°C at 760 mmHg
• Flash Point: 168.5°C
• Appearance: /
• Density: 1.032g/cm³
• Vapor Pressure: 3.31E-06mmHg at 25°C
• Refractive Index: 1.564
• CAS DataBase Reference: 2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE(108976-70-1)
• EPA Substance Registry System: 2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE(108976-70-1)

Safety Data

• Hazardous Substances Data: 108976-70-1(Hazardous Substances Data)

Usage

General Description

2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is a chemical compound with a molecular formula C16H16O that belongs to the class of ketones. It is a yellowish or off-white solid that is sparingly soluble in water but readily soluble in organic solvents. 2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is commonly used as a precursor in the synthesis of pharmaceuticals, flavoring agents, and fragrances. It is known for its sweet, floral, and fruity aroma, making it a valuable ingredient in perfumery. Additionally, 2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is also used as an intermediate in the production of dyes, polymers, and other organic compounds. Due to its versatile applications, this chemical is widely utilized in the chemical and pharmaceutical industries.

InChI:InChI=1/C17H18O/c1-13-8-9-14(2)16(12-13)17(18)11-10-15-6-4-3-5-7-15/h3-9,12H,10-11H2,1-2H3

Upstream product

• 106-42-3 para-xylene 
• 501-52-0 3-Phenylpropionic acid 
• 22422-19-1 3-chloro-1-(2,5-dimethylphenyl)propan-1-one 
• 98-80-6 phenylboronic acid 
• 2142-73-6 1-(2,5-dimethylphenyl)-1-ethanone 
• 100-51-6 benzyl alcohol 

Relevant articles and documents

A nanoscale iron catalyst for heterogeneous direct: N - And C -alkylations of anilines and ketones using alcohols under hydrogen autotransfer conditions

Here, we report a commercially available nanoscale Fe catalyst for heterogeneous direct N- and C-alkylation reactions of anilines and methyl ketones with alcohols. A hydrogen autotransfer mechanism has been found to operate in these reactions by deuterium labelling studies. In addition, dehydrogenative quinoline synthesis has been demonstrated from amino benzyl alcohols and acetophenones.

Organic Reactions Catalyzed by Solid Superacids. 5. Perfluorinated Sulfonic Acid Resin (Nafion-H) Catalyzed Intramolecular Friedel-Crafts Acylation

Nafion-H, a perfluorinated sulfonic acid resin, catalyzed the intramolecular Friedel-Crafts acylation of diarylalkane-2-carboxylic acids and arylalkanoic acids in refluxing p-xylene to provide cyclic ketones.The reactions were clean, and the water that was formed as a byproduct did not deactivate the catalyst.It was also found that the intramolecular acylation of the corresponding acid chlorides occurred under much milder reaction conditions.The mechanism of the reaction is discussed.