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化驗
98%
形狀
solid
mp
166-169 °C (lit.)
SMILES 字串
ClCc1ccc2C(=O)c3ccccc3C(=O)c2c1
InChI
1S/C15H9ClO2/c16-8-9-5-6-12-13(7-9)15(18)11-4-2-1-3-10(11)14(12)17/h1-7H,8H2
InChI 密鑰
NVUYDKYMEMGYFP-UHFFFAOYSA-N
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一般說明
2-(Chloromethyl)anthraquinone is an anthraquinone derivative. It was utilized as a substrate to synthesize Cibanone yellow R, a vat dye. Its electrochemical behavior has been studied over a wide pH range.
應用
2-(Chloromethyl)anthraquinone may be used in the following processes:
- Synthesis of 2-[methylamino-N-(1′-methyl-4′-N,N-diethylaminobutyl)]anthraquinone diphosphate.
- Synthesis of 2-(3,4-dicyano-phenyl)-2-(9,10-dioxo-9,10-dihydroantracen-2-yl-methyl)-malonic acid diethyl ester, starting reagent for the synthesis of tetra substituted metallophthalocyanines.
- To alter the glassy carbon (GC) electrode surface in order to investigate the oxygen reduction reaction (ORR) in alkaline medium.
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Proceedings of the Indian Academy of Sciences - Section A, 30(1) (1949)
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Synthesis, electrochemistry, spectroelectrochemistry and electrocolorimetry of phthalocyanine-anthraquinone hybrids.
Synt. Metals, 160(19), 2155-2166 (2010)
Electrochemical investigations of unexplored anthraquinones and their DNA binding.
Journal of Electrochemical Science and Engineering, 3(1), 19-27 (2013)
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