444650
2-Bromomethyl-anthraquinone
97%
Synonym(s):
MAQ-Br
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About This Item
Empirical Formula (Hill Notation):
C15H9BrO2
CAS Number:
Molecular Weight:
301.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2276854
Assay:
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
Related Categories
signalword
Warning
hcodes
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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Antitermite properties of some anthraquinone derivatives.
Gupta BK and Sen-Sarma PK.
Holzforschung, 30(3), 57-58 (1978)
Graphene: Large scale chemical functionalization by cathodic means.
Jouikov V and Simonet J.
Electrochemical Communications, 46, 132-136 (2014)
Inclusion of anthraquinone derivatives by the cucurbit [7] uril host.
Sindelar V, et al.
New. J. Chem., 31(5), 725-728 (2007)
Some Organic-Inorganic Hybrid Compounds Based on iso-Thiuronium Cations and Lead Halide Anions.
Papavassiliou GC, et al.
Zeitschrift fur Naturforschung (2001)
Modified carbon nanoparticle-chitosan film electrodes: Physisorption versus chemisorption.
Rassaei L, et al.
Electrochimica Acta, 53(19), 5732-5738 (2008)
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