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1,3-Dimethoxybenzene is an organic compound with the formula C 6 H 4 (OCH 3) 2. It is one of three isomers of dimethoxybenzene. Uses. 1,3-Dimethoxybenzene has been ...
1,3-Dimethoxybenzene 1,4-Dimethoxybenzene Structural Formula: CAS Registry Number: 91-16-7 151-10-0 150-78-7 All isomers share the molecular weight 138.17 g/mol and ...
It occurs naturally in willow (), tea, hyacinth, zucchini (Cucurbita pepo). [3] It appears to attract bees as it has a powerful response in their antenna. [4] In a study in mice, Iranian scientists identified 1,4-dimethoxybenzene as the major psychoactive chemical in musk willow (Salix aegyptiaca) by its ability to cause somnolescence and depressed activity.
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
1,2-Dimethoxybenzene, commonly known as veratrole, is an organic compound with the formula C 6 H 4 (OCH 3) 2. It is one of three isomers of dimethoxybenzene. It is a colorless liquid, with a pleasant odor and slight solubility in water. It is the dimethyl ether derived from pyrocatechol.
1,3-Dimethoxybenzene; 1,4-Dimethoxybenzene; Phenoxyethanol; Tyrosol; 1-phenyl-1,2-ethanediol This page was last edited on 7 July 2018, at 13:10 ...
The p-stands for para-, indicating that the two methyl groups in p-xylene occupy the diametrically opposite substituent positions 1 and 4. It is in the positions of the two methyl groups, their arene substitution pattern, that it differs from the other isomers, o-xylene and m-xylene. All have the same chemical formula C 6 H 4 (CH 3) 2. All ...
Piperonal can be prepared by the oxidative cleavage of isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene.Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent.