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Merck
CN

444650

2-Bromomethyl-anthraquinone

97%

Synonym(s):

MAQ-Br

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About This Item

Empirical Formula (Hill Notation):
C15H9BrO2
CAS Number:
7598-10-9
Molecular Weight:
301.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24868134
MDL number:
MFCD00042958
Beilstein/REAXYS Number:
2276854

Key Documents

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Product Name

2-Bromomethyl-anthraquinone, 97%

InChI

1S/C15H9BrO2/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

BrCc1ccc2C(=O)c3ccccc3C(=O)c2c1

InChI key

FCETXLHFBYOVCV-UHFFFAOYSA-N

assay

97%

mp

203 °C (dec.) (lit.)

functional group

bromo
ketone

Quality Level

200

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GHS07

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Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000464045
0000464045
0000427825
0000427825
0000335378

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Modified carbon nanoparticle-chitosan film electrodes: Physisorption versus chemisorption.
Rassaei L, et al.
Electrochimica Acta, 53(19), 5732-5738 (2008)
Some Organic-Inorganic Hybrid Compounds Based on iso-Thiuronium Cations and Lead Halide Anions.
Papavassiliou GC, et al.
Zeitschrift fur Naturforschung (2001)
Efficient immobilization of 9, 10-anthraquinonyl moiety at solid interfaces through 2-(bromomethyl) anthraquinone one-electron cleavage.
Jouikov V and Simonet J.
Electrochemical Communications, 27, 180-183 (2013)
Inclusion of anthraquinone derivatives by the cucurbit [7] uril host.
Sindelar V, et al.
New. J. Chem., 31(5), 725-728 (2007)
Antitermite properties of some anthraquinone derivatives.
Gupta BK and Sen-Sarma PK.
Holzforschung, 30(3), 57-58 (1978)
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