65800
2-Methylanthraquinone
technical, ≥95% (HPLC)
Synonym(s):
2-MAQ
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About This Item
Empirical Formula (Hill Notation):
C15H10O2
CAS Number:
Molecular Weight:
222.24
Beilstein/REAXYS Number:
2050523
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical
Quality Level
assay
≥95% (HPLC)
impurities
3-4% 1-methylanthraquinone
bp
236-238 °C/10 mmHg (lit.)
mp
170-173 °C (lit.)
functional group
ketone
SMILES string
Cc1ccc2C(=O)c3ccccc3C(=O)c2c1
InChI
1S/C15H10O2/c1-9-6-7-12-13(8-9)15(17)11-5-3-2-4-10(11)14(12)16/h2-8H,1H3
InChI key
NJWGQARXZDRHCD-UHFFFAOYSA-N
Gene Information
human ... CTSG(1511) , ELA2(1991)
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Application
2-Methylanthraquinone may be used in the preparation of potential bioreducible anthraquinone derivatives.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
408.2 °F - closed cup
flash_point_c
209 °C - closed cup
ppe
Eyeshields, Gloves
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Maria Helena Verdan et al.
Journal of natural products, 73(8), 1434-1437 (2010-08-06)
Three new aromatic epsilon-lactones, aggregatins A (1), B (2), and C (3), a new naphthoquinone derivative, aggregatin D (4), and three known anthraquinones, 2-methylanthraquinone, 7-methoxy-2-methylanthraquinone, and 7-hydroxy-2-methylanthraquinone, were isolated from the tubers of Sinningia aggregata (Gesneriaceae). Compounds 1 and 4
Helen Sheridan et al.
Journal of natural products, 74(1), 82-85 (2010-12-23)
Two new furanonaphthoquinones, (3R)-7-methoxy-α-dunnione (5) and (3R)-6-hydroxy-7-methoxy-α-dunnione (6), along with the known (3R)-dunnione (1), (3R)-α-dunnione (2), (3R)-7-hydroxy-α-dunnione (3), and 1-hydroxy-2-methylanthraquinone (4), were isolated from in vitro cultures of Streptocarpus dunnii. The structures of compounds 5 and 6 were established by
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
Lin TS, et al.
Journal of Medicinal Chemistry, 23(11), 1237-1242 (1980)
Emily L Whitson et al.
Journal of natural products, 75(3), 394-399 (2012-02-09)
Barleria alluaudii and Diospyros maritima were both investigated as part of an ongoing search for synergistic TRAIL (tumor necrosis factor-α-related apoptosis-inducing ligand) sensitizers. As a result of this study, two naphthoquinone epoxides, 2,3-epoxy-2,3-dihydrolapachol (1) and 2,3-epoxy-2,3-dihydro-8-hydroxylapachol (2), both not previously
Giampaolo Gori et al.
The Annals of occupational hygiene, 53(1), 27-32 (2008-11-04)
A new gas chromatographic/mass spectrometric (GC/MS) method was developed to detect 2-methylanthraquinone (2-MeA) in wood dust. 2-MeA is present in teak wood (a suspected human carcinogen) but not in oak, beech, mahogany, birch, ash or pine. The method involved collection
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