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Merck

65800

Sigma-Aldrich

2-甲基蒽醌

technical, ≥95% (HPLC)

别名:

2-MAQ

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About This Item

经验公式(希尔记法):
C15H10O2
CAS号:
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.)

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

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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


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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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