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Key Documents

65800

Sigma-Aldrich

2-甲基蒽醌

technical, ≥95% (HPLC)

同義詞:

2-MAQ

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About This Item

經驗公式(希爾表示法):
C15H10O2
CAS號碼:
分子量::
222.24
Beilstein:
2050523
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

technical

品質等級

化驗

≥95% (HPLC)

雜質

3-4% 1-methylanthraquinone

bp

236-238 °C/10 mmHg (lit.)

mp

170-173 °C (lit.)

官能基

ketone

SMILES 字串

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 密鑰

NJWGQARXZDRHCD-UHFFFAOYSA-N

基因資訊

尋找類似的產品? 前往 產品比較指南

應用

2-甲基蒽醌可用于制备潜在的生物可还原蒽醌衍生物。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

408.2 °F - closed cup

閃點(°C)

209 °C - closed cup

個人防護裝備

Eyeshields, Gloves


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分析證明 (COA)

Lot/Batch Number

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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
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
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
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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