四氯邻苯二酚
外观
四氯邻苯二酚 | |
---|---|
别名 | 3,4,5,6-Tetrachloro-1,2-benzenediol, Tetrachloropyrocatechol |
识别 | |
CAS号 | 1198-55-6 |
PubChem | 14537 |
ChemSpider | 13880 |
SMILES |
|
Beilstein | 1876366 |
Gmelin | 3937 |
ChEBI | 26889 |
KEGG | C18240 |
性质 | |
化学式 | C6H2Cl4O2 |
摩尔质量 | 247.89 g·mol−1 |
外观 | 白色固体 |
密度 | 1.848 g/cm3 (20 °C) |
熔点 | 194 °C(467 K) |
危险性 | |
GHS危险性符号 | |
GHS提示词 | Danger |
H-术语 | H302, H318, H400 |
P-术语 | P264, P264+265, P270, P273, P280, P301+317, P305+354+338, P317, P330, P391, P501 |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
四氯邻苯二酚是一种有机氯化合物,化学式为C
6Cl
4(OH)
2,它是白色固体,由五氯酚的降解产生。[1]它可由四氯邻苯醌和1-甲基-1,4-环己二烯[2]或二硼酸[3]的还原反应制得。它是TRISPHAT的前驱体。它的共轭碱可作为过渡金属的配体。[4]
参考文献
[编辑]- ^ Oturan, Mehmet A.; Oturan, Nihal; Lahitte, Claude; Trevin, Stéphane. Production of hydroxyl radicals by electrochemically assisted Fenton's reagent. Journal of Electroanalytical Chemistry. 2001, 507 (1–2): 96–102. doi:10.1016/S0022-0728(01)00369-2.
- ^ Andrea Baschieri, Riccardo Amorati, Luca Valgimigli, Letizia Sambri. 1-Methyl-1,4-cyclohexadiene as a Traceless Reducing Agent for the Synthesis of Catechols and Hydroquinones. The Journal of Organic Chemistry. 2019-11-01, 84 (21): 13655–13664 [2023-02-16]. ISSN 0022-3263. doi:10.1021/acs.joc.9b01898. (原始内容存档于2023-02-16) (英语).
- ^ Henian Peng, Tiejun Li, Duanshuai Tian, He Yang, Guangqing Xu, Wenjun Tang. Metal-free reduction of unsaturated carbonyls, quinones, and pyridinium salts with tetrahydroxydiboron/water. Organic & Biomolecular Chemistry. 2021, 19 (19): 4327–4337 [2023-02-16]. ISSN 1477-0520. doi:10.1039/D1OB00300C (英语).
- ^ Ackermann, Jens; Meyer, Franc; Kaifer, Elisabeth; Pritzkow, Hans. Tuning the Activity of Catechol Oxidase Model Complexes by Geometric Changes of the Dicopper Core. Chemistry - A European Journal. 2002, 8 (1): 247–258. PMID 11822456. doi:10.1002/1521-3765(20020104)8:1<247::AID-CHEM247>3.0.CO;2-P.