18272-61-2

Usage

Type of compound

Phenolic compound

Usage

Antioxidant and preservative in industries such as food, cosmetics, and pharmaceuticals

Physical state

Yellow liquid

Odor

Characteristic phenolic odor

Solubility

Soluble in alcohol and ether

Antimicrobial properties

Prevents the growth of mold and bacteria

Use in synthesis

Used in the synthesis of other chemical compounds

Fragrance ingredient

Used in perfumes and soaps

Safety precautions

Can be irritating to skin and eyes; prolonged exposure should be avoided.

Upstream product

• 59671-72-6 2-(1',1'-dimethylprop-2'-enyl)phenyl acetate 
• 556-82-1 3-methyl-2-buten-1-ol 
• 108-95-2 phenol 
• 503-60-6 3,3-dimethyl-allyl chloride 
• 139-02-6 sodium phenoxide 
• 19493-09-5 Methylenetriphenylphosphorane 
• 14309-15-0 phenyl prenyl ether 

Downstream Products

• 139437-09-5 4-(2'-hydroxyphenyl)-4-methylpentanal 
• 139437-10-8 5,5-dimethyl-2,3,4,5-tetrahydro-1-benzoxepin-2-ol 

Relevant academic research and scientific papers

Alkylation of Phenol And Hydroquinone by Prenol in the Presence of Organoaluminum Catalysts

Prenylphenols and 2,2-dimethylbenzopyrans were synthesized via alkylation of phenol and hydroquinone with prenol in the presence of organoaluminum catalysts, i.e., aluminum phenoxide and isopropoxide. Reaction products were isolated and characterized. Sev

InIII-catalysed tandem C-C and C-O bond formation between phenols and allylic acetates

Indium triflate catalysed tandem allylation-intramolecular hydroalkoxylation was efficiently carried out by using 1 mol-% of the catalyst under mild conditions to afford the dihydrobenzopyran ring system (chroman-type structure) in good yields. Kinetic, mechanistic and theoretical studies are also presented. Tandem allylation-intramolecular hydroalkoxylation carried out in the presence of an indium catalyst (1 mol-%) under mild conditions provides the dihydrobenzopyranring system in good yields. Kinetic, mechanistic and theoretical studies are presented.

Heteroaryl compounds as P2Y1 receptor inhibitors

The present invention provides novel heteroaryl compounds and analogues thereof, which are selective inhibitors of the human P2Y1 receptor. The invention also provides for various pharmaceutical compositions of the same and methods for treating diseases responsive to modulation of P2Y1 receptor activity.

The Stereochemistry of Organometallic Compounds. XXXV. Hydroformylation of ortho-Propenylanilines and ortho-Propenylphenols: a New Route to 4,5-Dihydro-3H-1-benzazepines

Rhodium-catalyzed hydroformylation of readily available ortho-propenylanilines gives 4,5-dihydro-3H-1-benzazepines together with small amounts of substituted 3-methylquinolines (15percent).The regioselectivity of these reactions and the hydroformylation of related ortho-propenylphenols are discussed.