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434256

Sigma-Aldrich

2-(Chloromethyl)anthraquinone

98%

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About This Item

Empirical Formula (Hill Notation):
C15H9ClO2
CAS Number:
Molecular Weight:
256.68
Beilstein/REAXYS Number:
1975355
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

166-169 °C (lit.)

functional group

chloro
ketone

SMILES string

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 key

NVUYDKYMEMGYFP-UHFFFAOYSA-N

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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.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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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)
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)
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)

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