65800
2-甲基蒽醌
technical, ≥95% (HPLC)
别名:
2-MAQ
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关于此项目
经验公式（希尔记法）:
C15H10O2
化学文摘社编号:
分子量:
222.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-539-6
Beilstein/REAXYS Number:
2050523
MDL number:
产品名称
2-甲基蒽醌, technical, ≥95% (HPLC)
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
SMILES string
Cc1ccc2C(=O)c3ccccc3C(=O)c2c1
grade
technical
assay
≥95% (HPLC)
impurities
3-4% 1-methylanthraquinone
bp
236-238 °C/10 mmHg (lit.)
mp
170-173 °C (lit.)
functional group
ketone
Quality Level
Gene Information
human ... CTSG(1511), ELA2(1991)
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Application
2-甲基蒽醌可用于制备潜在的生物可还原蒽醌衍生物。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
408.2 °F - closed cup
flash_point_c
209 °C - closed cup
ppe
Eyeshields, Gloves
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
Effect of additives on fiber yield improvement for kraft pulping of kadam (Anthocephalus chinensis).
D Biswas et al.
Bioresource technology, 102(2), 1284-1288 (2010-09-11)
Projected decline in future wood resources has prompted researchers to try various additives in existing pulping processes for fiber yield improvement. Many studies have been conducted in the past aimed at improving kraft pulp yield with the use of additives
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
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
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
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