431982
2,6-二氯-1,4-苯醌
98%
别名:
2,6-二氯-2,5-环己二烯-1,4-二酮, 2,6-二氯对苯醌
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关于此项目
经验公式（希尔记法）:
C6H2Cl2O2
化学文摘社编号:
分子量:
176.98
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-810-0
MDL number:
产品名称
2,6-二氯-1,4-苯醌, 98%
InChI key
JCARTGJGWCGSSU-UHFFFAOYSA-N
InChI
1S/C6H2Cl2O2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H
SMILES string
ClC1=CC(=O)C=C(Cl)C1=O
assay
98%
mp
122-124 °C (lit.)
Quality Level
Application
2,6-二氯-1,4-苯醌可作为一种适用的试剂，用于通过单电位步进计时电流法对乙腈中的醌、硝基芳族化合物、二茂铁和芳烃化合物家族扩散系数（D）进行研究。它可用于制备：
- 2,3,5-三氯-1,4-二氢醌
- 2,3,5-三氯-1,4-苯醌
- 2,6-二氯-1,4-二氢醌
General description
2,6-二氯-1,4-苯醌（DCBQ，2,6-DCBQ）是一种卤代苯醌。卤代苯醌是在饮用水中发现的一类消毒副产物（DBP）。它们能够产生活性氧，并对T24人膀胱癌细胞中的蛋白和DNA造成氧化损伤。紫外线所引起的饮用水中DCBQ的转化已被报道。已报道可通过液相色谱-ESI串联质谱法检测饮用水中的DCBQ。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Jinhua Li et al.
Toxicological sciences : an official journal of the Society of Toxicology, 141(2), 335-343 (2014-05-09)
Halobenzoquinones (HBQs) are a new class of drinking water disinfection byproducts (DBPs) and are capable of producing reactive oxygen species and causing oxidative damage to proteins and DNA in T24 human bladder carcinoma cells. However, the exact mechanism of the
Kai He et al.
Journal of hazardous materials, 351, 98-107 (2018-03-10)
Anthropogenic compounds accidentally released to the environment could be important precursors of disinfection byproducts (DBPs) in drinking water treatment processes. In this study, the haloacetic acid formation potentials (HAAFPs) of 155 anthropogenic compounds listed on the Japanese pollutant release and
Y I Park et al.
FEBS letters, 444(1), 102-105 (1999-02-26)
Intracellular carbonic anhydrases (CA) in aquatic photosynthetic organisms are involved in the CO2-concentrating mechanism (CCM), which helps to overcome CO2 limitation in the environment. In the green alga Chlamydomonas reinhardtii, this CCM is initiated and maintained by the pH gradient
N Knoepfle et al.
Biochemistry, 38(5), 1582-1588 (1999-02-04)
The intrinsic chlorophyll protein CP 43, a component of photosystem II (PS II) in higher plants, green algae, and cyanobacteria, is encoded by the psbC gene. Oligonucleotide-directed mutagenesis was employed to introduce mutations into a segment of psbC that encodes
A A Leontievsky et al.
Biodegradation, 11(5), 331-340 (2001-08-07)
The toxicity of thirteen isomers of mono-, di-, tri- and pentachlorophenols was tested in potato-dextrose agar cultures of the white rot fungi Panus tigrinus and Coriolus versicolor. 2,4,6-Trichlorophenol (2,4,6-TCP) was chosen for further study of its toxicity and transformation in
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