推薦產品
品質等級
化驗
98%
mp
160-163 °C (lit.)
官能基
chloro
ketone
SMILES 字串
ClC1=CC(=O)C(Cl)=CC1=O
InChI
1S/C6H2Cl2O2/c7-3-1-5(9)4(8)2-6(3)10/h1-2H
InChI 密鑰
LNXVNZRYYHFMEY-UHFFFAOYSA-N
一般說明
2,5-二氯-1,4-苯醌 (DCBQ) 是一种卤代醌。DCBQ 是致癌中间体。他们在饮用水中发现了氯化消毒副产物。据报道,DCBQ 通过形成 t -丁氧基自由基,增加了模型 ROOH 叔 -丁基过氧化氢的分解。用量子化学方法研究了 DCBQ 二聚体的异构体之间的非共价键相互作用。已经通过实验以及理论电荷密度分析研究了存在于 2,5-二氯-1,4-苯醌中的卤素键。已研究了其与吡咯烷的反应。
應用
2,5-二氯-1,4-苯醌可用于以下过程:
- 作为合成菊醌 D 的起始原料。
- 作为研究具有 LED(发光二极管)光源和光纤 CCD(电荷耦合器件)分光光度计的新型光反应器的实用性的模型。
- 钯催化吲哚合成 2,5-二氯-3,6-二(3-吲哚基)-1,4-对苯二酚。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
客戶也查看了
Physical chemistry chemical physics : PCCP, 16(37), 19928-19940 (2014-08-15)
The competition between non-covalent interactions (NCIs), such as C-H∙∙∙O, C-H∙∙∙Cl, C-Cl∙∙∙O, C-Cl∙∙∙Cl-C, C-O∙∙∙C, C-Cl∙∙∙C and C-O∙∙∙π, in the isomers of the 2,5-dichloro-1,4-benzoquinone (DCBQ) dimer were investigated by quantum chemical calculations to study the properties of the ground and excited states.
Halogen bonding in 2, 5-Dichloro-1, 4-benzoquinone: Insights from experimental and theoretical charge density analysis.
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Halogenated quinones (XQ) are a class of carcinogenic intermediates and newly identified chlorination disinfection byproducts in drinking water. Organic hydroperoxides (ROOH) can be produced both by free radical reactions and enzymatic oxidation of polyunsaturated fatty acids. ROOH have been shown
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(4), 519-526 (2016-12-13)
Substituted 1,4-benzoquinone (QR) derivatives are photosensitive in aqueous solution and form hydroquinones (QR-H
Construction of a photochemical reactor combining a CCD spectrophotometer and a LED radiation source.
Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society for Photobiology, 11(10), 1592-1595 (2012)
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