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等級
technical
化驗
≥95% (HPLC)
雜質
3-4% 1-methylanthraquinone
bp
236-238 °C/10 mmHg (lit.)
mp
170-173 °C (lit.)
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
human ... CTSG(1511) , ELA2(1991)
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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
其他客户在看
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
Journal of Medicinal Chemistry, 23(11), 1237-1242 (1980)
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 16(11), 675-676 (1991-11-01)
This paper reports the identification of four compounds isolated from the cortex of Morinda officinalis growing in Guangdong Province. These compounds are beta-sitosterol (I), 2-methyl-anthraquinone(II), rubiadin-1-methyl ether(III) and 24-ethylcholesterol(VI). Compounds II and VI are isolated from Morinda Genus for the
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
Effect of additives on fiber yield improvement for kraft pulping of kadam (Anthocephalus chinensis).
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
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
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