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444650

Sigma-Aldrich

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
Beilstein:
2276854
MDL number:
MFCD00042958
UNSPSC Code:
12352100
PubChem Substance ID:
24868134
NACRES:
NA.22

Assay

97%

mp

203 °C (dec.) (lit.)

functional group

bromo
ketone

SMILES string

BrCc1ccc2C(=O)c3ccccc3C(=O)c2c1

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

InChI key

FCETXLHFBYOVCV-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000335378
0000324100
BGBB9401
1452276V

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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)
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)
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