434256
2-氯乙基蒽
98%
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关于此项目
经验公式（希尔记法）:
C15H9ClO2
化学文摘社编号:
分子量:
256.68
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1975355
Assay:
98%
Form:
solid
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
SMILES string
ClCc1ccc2C(=O)c3ccccc3C(=O)c2c1
InChI key
NVUYDKYMEMGYFP-UHFFFAOYSA-N
assay
98%
form
solid
mp
166-169 °C (lit.)
functional group
chloro, ketone
Quality Level
General description
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.
Application
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.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Kevin K Schrader et al.
Applied and environmental microbiology, 69(9), 5319-5327 (2003-09-06)
Musty "off-flavor" in pond-cultured channel catfish (Ictalurus punctatus) costs the catfish production industry in the United States at least 30 million US dollars annually. The cyanobacterium Oscillatoria perornata (Skuja) is credited with being the major cause of musty off-flavor in
Sulphur dyes and sulphurised vat dyes.
Shah KH, et al.
Proceedings of the Indian Academy of Sciences - Section A, 30(1) (1949)
Electrocatalysis of oxygen reduction on glassy carbon electrodes modified with anthraquinone moieties.
Mooste M, et al.
Journal of Solid State Electrochemistry, 18(6), 1725-1733 (2014)
Electrochemical investigations of unexplored anthraquinones and their DNA binding.
Shah A, et al.
Journal of Electrochemical Science and Engineering, 3(1), 19-27 (2013)
Synthesis, electrochemistry, spectroelectrochemistry and electrocolorimetry of phthalocyanine-anthraquinone hybrids.
Sezer B, et al.
Synt. Metals, 160(19), 2155-2166 (2010)
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