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Merck
CN

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
Beilstein:
2050523
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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等级

technical

质量水平

方案

≥95% (HPLC)

杂质

3-4% 1-methylanthraquinone

沸点

236-238 °C/10 mmHg (lit.)

mp

170-173 °C (lit.)

官能团

ketone

SMILES字符串

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 key

NJWGQARXZDRHCD-UHFFFAOYSA-N

基因信息

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应用

2-甲基蒽醌可用于制备潜在的生物可还原蒽醌衍生物。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

408.2 °F - closed cup

闪点(°C)

209 °C - closed cup

个人防护装备

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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S Li et al.
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
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
Lin TS, et al.
Journal of Medicinal Chemistry, 23(11), 1237-1242 (1980)
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

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