Search results
Results from the WOW.Com Content Network
2-Phenylphenol is a precursor to 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, a commercial fire retardant. The sodium salt of orthophenyl phenol, sodium orthophenyl phenol, is a preservative, used to treat the surface of citrus fruits. [5] Orthophenyl phenol is also used as a fungicide in food packaging and may migrate into the contents. [6]
Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils. It is slightly soluble in water (2 ml per 100 ml of H 2 O), but miscible with most organic solvents.
Phenol esters are active esters, being prone to hydrolysis. Phenols are reactive species toward oxidation. Oxidative cleavage, for instance cleavage of 1,2-dihydroxybenzene to the monomethylester of 2,4 hexadienedioic acid with oxygen, copper chloride in pyridine [4] Oxidative de-aromatization to quinones also known as the Teuber reaction.
Monosubstituted phenyl groups (that is, disubstituted benzenes) are associated with electrophilic aromatic substitution reactions and the products follow the arene substitution pattern. So, a given substituted phenyl compound has three isomers, ortho (1,2-disubstitution), meta (1,3-disubstitution) and para (1,4-disubstitution). A disubstituted ...
2-Phenylethyl acetate. Other names Phenethyl acetate. Identifiers CAS Number. 103-45-7; 3D model . ... This page was last edited on 1 October 2020, at 09:06 (UTC).
The long-chain alkylphenols are prepared by alkylation of phenol with alkenes: C 6 H 5 OH + RR'C=CH2 → RR'CH−CH 2 −C 6 H 4 OH. In this way, about 500M kg/y are produced. Alkylphenols ethoxylates are common surfactants. Long-chain alkylphenols are used extensively as precursors to detergents.
2-Hydroxybenzoic acid, others 138.031694 C6H6O4: 1,2,3,5-Tetrahydroxybenzene 142.026608 C9H6O2: Coumarin 146.036779 C9H8O2: Cinnamic acid 148.05243 C9H10O2: 2-Methoxy-4-vinylphenol, others 150.06808 C10H14O: Carvacrol 150.104465 C8H8O3: 4-Hydroxyphenylacetic acid, others 152.047344 C9H12O2: 4-Ethylguaiacol 152.083729 C7H6O4: Protocatechuic acid ...
Usually phenol ethers are synthesized through the condensation of phenol and an organic alcohol; however, other known reactions regarding the synthesis of ethers can be applied to phenol ethers as well. Anisole (C 6 H 5 OCH 3) is the simplest phenol ether, and is a versatile precursor for perfumes and pharmaceuticals. [1]