1197-34-8

Basic information

• Product Name: 3,5-diethylphenol
• Synonyms: 3,5-diethylphenol
• CAS NO: 1197-34-8
• Molecular Formula: C₁₀H₁₄O
• Molecular Weight: 150.21756
• EINECS: 214-824-5
• Mol File: 1197-34-8.mol
• Article Data: 8

Chemical Properties

• Melting Point: 76°C
• Boiling Point: 248°C
• Flash Point: 114.7°C
• Appearance: /
• Density: 0.9688 (estimate)
• Vapor Pressure: 0.0115mmHg at 25°C
• Refractive Index: 1.5091 (estimate)
• CAS DataBase Reference: 3,5-diethylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-diethylphenol(1197-34-8)
• EPA Substance Registry System: 3,5-diethylphenol(1197-34-8)

Safety Data

• Hazardous Substances Data: 1197-34-8(Hazardous Substances Data)

Usage

General Description

3,5-diethylphenol is a chemical compound with the molecular formula C10H14O. It is a colorless, slightly viscous liquid with a sweet, floral odor. 3,5-diethylphenol is commonly used as a fragrance ingredient and as a raw material in the production of various chemicals and pharmaceuticals. It is also utilized in the manufacturing of resins, adhesives, and coatings. Additionally, 3,5-diethylphenol exhibits antioxidant properties and is used as a stabilizer in the production of polymer materials. Due to its potential health hazards, 3,5-diethylphenol should be handled and stored with care, and exposure to this chemical should be minimized.

InChI:InChI=1/C10H14O/c1-3-8-5-9(4-2)7-10(11)6-8/h5-7,11H,3-4H2,1-2H3

Upstream product

• 7446-70-0 aluminium trichloride 
• 60-29-7 diethyl ether 
• 108-95-2 phenol 
• 620-17-7 3-ethylphenol 
• 64-17-5 ethanol 
• 90-05-1 2-methoxy-phenol 
• 120-80-9 benzene-1,2-diol 
• 94-71-3 2-Ethoxyphenol 
• 150-76-5 4-methoxy-phenol 
• 202858-61-5 dimethyl 4,6-diethyl-2-hydroxyisophthalate 
• 906623-13-0 4,6-diethyl-2-hydroxyisophthalic acid 
• 86119-84-8 phosphoric acid 
• 575487-29-5 1-(2,4-diethyl-6-hydroxy-phenyl)-ethanone 
• 123-07-9 4-Ethylphenol 

Downstream Products

• 58276-40-7 Methyl-(1-methylsulfanyl-vinyl)-carbamic acid 3,5-diethyl-phenyl ester 
• 52328-45-7 3,5-diethyl-anisole 
• 51202-02-9 2,4,6-Trichlor-3,5-diethylphenol 
• 18102-51-7 1-Aethoxy-3,5-diaethylphenol 
• 18102-07-3 3-Methyl-5-propylphenetole 
• 18102-08-4 3,5-Dipropylphenetole 
• 110457-73-3 3,5-dipropyl-2-ethylphenetole 
• 110457-78-8 3,5-dipropyl-4-ethylphenetole 
• 110457-76-6 5-propyl-3-(1-ethylpropyl)phenetole 
• 26489-77-0 2-Allyl-3,5-diethyl-phenol 
• 52145-48-9 Methyl-carbamic acid 4-(4-chloro-phenylsulfanyl)-3,5-diethyl-phenyl ester 
• 52145-47-8 Methyl-carbamic acid 3,5-diethyl-4-phenylsulfanyl-phenyl ester 
• 103095-65-4 3,5-diethyl-4-nitro-phenol 
• 50348-20-4 2,6-diethyl-1,4-benzoquinone 

Relevant articles and documents

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Method for preparing hydrocarbyl phenol by catalytic conversion of phenolic compound in presence of molybdenum-based catalyst

The invention discloses a method for preparing hydrocarbyl phenol by catalytic conversion of a phenolic compound in the presence of a molybdenum-based catalyst. The method comprises mixing a phenoliccompound, a molybdenum-based catalyst and a reaction solvent, adding the mixture into a sealed reactor, feeding gas into the reactor, heating the mixture to 150-350 DEG C, carrying out stirring for areaction for 0.5-2h, then filtering to remove a solid catalyst and carrying out rotary evaporateion to obtain a liquid product. The phenolic compound has a wide source, a cost is low, product alkyl phenol selectivity is high, an added value is high, alcohol or an alcohol-water mixture is used as a reaction solvent, environmental friendliness is realized, pollution is avoided, any inorganic acids and alkalis are avoided in the reaction process, the common environmental pollution problems in the biomass processing technology are solved, the reaction conditions are mild, the process can be carried out at a low temperature, high-efficiency conversion of the reactants can be realized without consuming hydrogen gas and the method is suitable for large-scale industrial trial production.

FUSED CYCLIC COMPOUNDS

The present invention provides a compound represented by the formula (I): wherein each symbol is as defined in the description, or a salt thereof. The compound or a salt thereof or a prodrug thereof has a GPR40 receptor function modulating action and is useful as an insulin secretagogue or an agent for the prophylaxis or treatment of diabetes and the like.