D67200
2,3-二氯-1,4-萘醌
98%
别名:
二氯萘醌
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关于此项目
经验公式（希尔记法）:
C10H4Cl2O2
化学文摘社编号:
分子量:
227.04
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-210-5
Beilstein/REAXYS Number:
1073511
MDL number:
Assay:
98%
Form:
powder
InChI key
SVPKNMBRVBMTLB-UHFFFAOYSA-N
InChI
1S/C10H4Cl2O2/c11-7-8(12)10(14)6-4-2-1-3-5(6)9(7)13/h1-4H
SMILES string
ClC1=C(Cl)C(=O)c2ccccc2C1=O
assay
98%
form
powder
mp
194-197 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
农药列管产品
危险化学品
此项目有
Avijit Saha et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(3), 835-840 (2008-03-18)
4-Acetamidophenol (paracetamol) is shown to form charge transfer complex with 2,3-dichloro1,4-naphthoquinone in aqueous ethanol media exhibiting the unusual 2:1 (paracetamol:quinone) stoichiometry. The complexation enthalpy and entropy have been estimated from the formation constant (K) determined spectrophotometrically at five different temperatures.
Vishnu K Tandon et al.
European journal of medicinal chemistry, 44(3), 1086-1092 (2008-08-19)
A series of 2-chloro-3-arylsulfanyl-[1,4]naphthoquinones (2), 2,3-bis-arylsulfanyl-[1,4]naphthoquinones (3) and 12H-benzo[b]phenothiazine-6,11-diones and their analogs 6-8 were synthesized and evaluated for their antiproliferative activity against human cervical cancer (HeLa) cells. Compounds 3a and 3b were found to possess most potent antiproliferative and cell
S Ahmad et al.
Archives of environmental contamination and toxicology, 29(4), 442-448 (1995-11-01)
Southern armyworm, Spodoptera eridania, larvae were provided ad libitum 0.002-0.25% w/w dichlone, 2,3-dichloro-1,4-naphthoquinone (CNQ). Larval mortality occurred in a time-and-dose dependent manner, with an LC17 of 0.01% and an LC50 of 0.26% CNQ at day-5. Extracts of larvae fed control
Inhibition of liver glycolysis in rats by dietary dichlone (2,3-dichloro-1,4-naphthoquinone).
C A Pritsos et al.
Bulletin of environmental contamination and toxicology, 35(1), 23-28 (1985-07-01)
Angupillai Satheshkumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 98, 378-383 (2012-09-18)
Various spectroscopy techniques (UV-Vis, DRS, FT-IR, (1)H NMR, LC-MS) and theoretical computations have been employed to investigate the mechanism of the nucleophilic substitution reaction of 2,3-dichloronaphthoquinone (DCNQ) with para-substituted anilines in solid state under base- and solvent-free conditions against traditional
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