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Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C 6 H 5 OH. [5] It is a white crystalline solid that is volatile . The molecule consists of a phenyl group ( −C 6 H 5 ) bonded to a hydroxy group ( −OH ).
2,6-Di-tert-butylphenol is an organic compound with the structural formula 2,6-((CH 3) 3 C) 2 C 6 H 3 OH. This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and antioxidants for hydrocarbon-based products ranging from petrochemicals to plastics. [1] Illustrative of its usefulness, it prevents ...
In organic chemistry, 3-hydroxybutanal (acetaldol, aldol) is an organic compound with the formula CH 3 CH(OH)CH 2 CHO and the structure H 3 C−CH−CH 2 −CH=O. It is classified as an aldol (R−CH(OH)−CHR'−C(=O)−R") and the word "aldol" can refer specifically to 3-hydroxybutanal. It is formally the product of the dimerization of ...
Phenol is readily alkylated at the ortho positions using alkenes in the presence of a Lewis acid such as aluminium phenoxide: [citation needed] CH 2 =CR 2 + C 6 H 5 OH → R 2 CHCH 2 -2-C 6 H 4 OH More than 100,000 tons of tert-butyl phenols are produced annually (year: 2000) in this way, using isobutylene (CH 2 =CMe 2 ) as the alkylating agent.
2,4-Bis(4-hydroxybenzyl) phenol 306.125594 C16H20O6: Monocerin 308.1259876 C13H12O9: Caftaric acid 312.048132 C13H16O9: Norbergenin 314.063782 C17H14O6: Ermanin, others 314.079038 C18H18O5: Flavokavain A, others 314.115424 C17H15O6: Rosinidin 315.086863 C16H12O7: Isorhamnetin, others 316.058303 C19H24O4: Ferujol 316.167459 C18H20O5 ...
The general structure of a phenol ether. In chemistry, a phenol ether (or aromatic ether) is an organic compound derived from phenol (C 6 H 5 OH), where the hydroxyl (-OH) group is substituted with an alkoxy (-OR) group.
Both industrially and in the laboratory, propionaldehyde has primary application as a chemical building block. [2]: 4 [4] It is predominantly used as a precursor to trimethylolethane (CH 3 C(CH 2 OH) 3) through a condensation reaction with formaldehyde. This triol is an important intermediate in the production of alkyd resins.
Simplfied general structure of a resole. Base-catalysed phenol-formaldehyde resins are made with a formaldehyde to phenol ratio of greater than one (usually around 1.5). These resins are called resoles. Phenol, formaldehyde, water and catalyst are mixed in the desired amount, depending on the resin to be formed, and are then heated.