Tetrabromocatechol
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Tetrabromocatechol | ||||||||||||||||||
other names |
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Molecular formula | C 6 H 2 Br 4 O 2 | ||||||||||||||||||
Brief description |
whitish powder |
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properties | |||||||||||||||||||
Molar mass | 425.69 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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Melting point |
189-193 ° C |
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safety instructions | |||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Tetrabromopychol is a chemical compound that belongs to both the phenol group and the halogen aromatic compound .
presentation
Tetrabromopychol is produced by the bromination of catechol with potassium bromide and bromine .
Tetrabromo-catechol is also formed when protocatechuic acid is boiled with bromine.
properties
Tetrabromopychol crystallizes in colorless prisms. With nitric acid , tetrabromopyrocatechol is oxidized to tetrabromo- o -benzoquinone , which melts at 150–151 ° C and crystallizes in red prisms that are soluble in ethanol , ether and benzene .
Analytical evidence
An alcoholic solution of tetrabromopyrocatechol is colored dark blue by adding iron (III) chloride .
Individual evidence
- ↑ a b c data sheet tetrabromocatechol from Sigma-Aldrich , accessed on April 23, 2011 ( PDF ).
- ^ Dictionary of organic compounds, p. 932 ( limited preview in Google book search).
- ^ Association of authors: Organikum , 19th edition, Johann Ambrosius Barth, Leipzig · Berlin · Heidelberg 1993, ISBN 3-335-00343-8 , p. 653.
- ^ Association of authors: Organikum , 19th edition, Johann Ambrosius Barth, Leipzig · Berlin · Heidelberg 1993, ISBN 3-335-00343-8 , p. 331.
- ↑ a b c d H. E. Roscoe, C. Schorlemmer: "A treatise on chemistry", 1891, p. 154; Full text .
- ↑ Th. Zincke: "Ueber Derivate des Ortho-Benzochinons", in: Ber. d. German Chem. Ges. , 1887 , 20 , pp. 1776-1780; doi : 10.1002 / cber.188702001399 .