enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Fluorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzaldehyde

    2-Fluorobenzaldehyde 3-Fluorobenzaldehyde 4-Fluorobenzaldehyde Molecular formula: C 7 H 5 FO C 7 H 5 FO C 7 H 5 FO Molar mass: 124.11 g/mol 124.11 g/mol 124.11 g/mol CAS number: 446-52-6 456-48-4 459-57-4 EC number 207-171-2 207-266-9 459-57-4 Properties: Melting point-44.5°C -10°C Boiling point: 175°C 173°C 181°C Flash point: 55°C 56°C ...

  3. Mequinol - Wikipedia

    en.wikipedia.org/wiki/Mequinol

    Mequinol, MeHQ or 4-methoxyphenol, is an organic compound with the formula CH 3 OC 6 H 4 OH. It is a phenol with a methoxy group in the para position. A colorless solid, it is used in dermatology [1] and organic chemistry. [2]

  4. Methoxyphenol - Wikipedia

    en.wikipedia.org/wiki/Methoxyphenol

    Methoxyphenol or hydroxyanisole may refer to: 2-Methoxyphenol (guaiacol, o-methoxyphenol, methylcatechol, 2-hydroxyanisole) 3-Methoxyphenol (m-methoxyphenol, m ...

  5. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    Orcinol (5-methylbenzene-1,3-diol) Methoxyphenols — can be derived from benzenediols by O-methylation. Guaiacol (2-methoxyphenol, O-Methylcatechol) Mequinol (4-Methoxyphenol) Dimethoxybenzenes — can be derived from benzenediols by two rounds of O-methylation. Veratrole (1,2-Dimethoxybenzene) 1,3-Dimethoxybenzene; 1,4-Dimethoxybenzene

  6. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    The Cannizzaro reaction, named after its discoverer Stanislao Cannizzaro, is a chemical reaction which involves the base-induced disproportionation of two molecules of a non-enolizable aldehyde to give a primary alcohol and a carboxylic acid.

  7. Category:Benzaldehydes - Wikipedia

    en.wikipedia.org/wiki/Category:Benzaldehydes

    This page was last edited on 3 February 2020, at 01:59 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  8. 4-Hydroxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-hydroxybenzaldehyde

    4Hydroxy­benzaldehyde (para‑hydroxy­benzaldehyde) is an organic compound with the formula C 6 H 4 OH(CHO). [ 4 ] [ 5 ] Along with 2-hydroxybenzaldehyde and 3-hydroxybenzaldehyde , it is one of the three isomers of hydroxybenzaldehyde .

  9. Balz–Schiemann reaction - Wikipedia

    en.wikipedia.org/wiki/Balz–Schiemann_reaction

    The traditional Balz–Schiemann reaction employs HBF 4 and involves isolation of the diazonium salt. Both aspects can be profitably modified. Other counterions have been used in place of tetrafluoroborates, such as hexafluorophosphates (PF 6 −) and hexafluoroantimonates (SbF 6 −) with improved yields for some substrates.