I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
It is useful for organic synthesis of aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.
Biju M. Devassy.; S.B. Halligudi. Zirconia-supported heteropoly acids: Characterization and catalytic behavior in liquid-phase veratrole benzoylation.J. Catal. 2005, 236 (2),313-323.
Irene M. Matheson (née Davidson).;O. C. Musgrave.; C. J. Webster. Oxidation of veratrole by quinones. Chem. Commun. (London). 1965, (13), 278-279.
In contrast to 1,3-Dimethoxybenzene, A13380, direct dilithiation with n-BuLi + TMEDA is feasible, giving, after reaction with TMS chloride, the 3,6-disilyl derivative as the major product in 50-60% yield: J. Org. Chem., 49, 4657 (1984).
Hazard Statements: H302-H312-H332
Harmful if swallowed. Harmful in contact with skin. Harmful if inhaled.
Precautionary Statements: P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P312-P330-P363-P501c
Avoid breathing dust/fume/gas/mist/vapours/spray. Wash face, hands and any exposed skin thoroughly after handling Do not eat, drink or smoke when using this product. Use only outdoors or in a well-ventilated area. Wear protective gloves/protective clothing/eye protection/face protection. IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell. IF ON SKIN: Wash with plenty of soap and water. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Rinse mouth. Wash contaminated clothing before reuse. Dispose of contents/ container to an approved waste disposal plant