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Merck
CN

39579

Sigma-Aldrich

2,5-二甲基-对苯醌

≥98.0%

别名:

2,5-二甲基-2,5-环己二烯-1,4-二酮, 2,5-二甲基-p-醌, 2,5-二甲基对苯醌, 2,5-二甲基苯醌, 3,6-二甲基对苯醌

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关于此项目

经验公式(希尔记法):
C8H8O2
化学文摘社编号:
分子量:
136.15
Beilstein:
2041348
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案

≥98.0%

mp

123-125 °C

溶解性

toluene: soluble 0.5 g/10 mL, clear to faintly turbid, yellow to brown

官能团

ketone

SMILES字符串

CC1=CC(=O)C(C)=CC1=O

InChI

1S/C8H8O2/c1-5-3-8(10)6(2)4-7(5)9/h3-4H,1-2H3

InChI key

MYKLQMNSFPAPLZ-UHFFFAOYSA-N

一般描述

2,5-二甲基-1,4-苯醌是醌衍生物。在 pH 7.8 的磷酸盐缓冲液中研究了其与刀豆脲酶的反应。它是棘头虫防御性分泌的成分之一。在 pH 7.0 的 50 mM 磷酸盐缓冲液中,对其作为刀豆脲酶抑制剂进行了研究。

应用

2,5-二甲基-1,4-苯醌可能用于参与 (-) -胱抑素 A 3 全合成的关键步骤。

象形图

Skull and crossbones

警示用语:

Danger

危险分类

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Dale E Ward et al.
Organic letters, 9(15), 2843-2846 (2007-06-22)
The total synthesis of (-)-cyathin A3 is described. The key step involves an unusual enantioselective Diels-Alder reaction of 2,5-dimethyl-1,4-benzoquinone with 2,4-bis(trimethylsilyloxy)-1,3-pentadiene, using Mikami's catalyst [(R)-BINOL + Cl2Ti(OiPr)2 + 4 A mol sieves] modified by addition of Mg and SiO2. Because
Thomas Eisner et al.
The Journal of experimental biology, 207(Pt 8), 1313-1321 (2004-03-11)
The opilionid Acanthopachylus aculeatus was shown to produce a defensive secretion containing quinones (2,3-dimethyl-1,4-benzoquinone, 2,5-dimethyl-1,4-benzoquinone and 2,3,5-trimethyl-1,4-benzoquinone), confirming the findings reported nearly a half century ago in a classic study. The mechanism by which the opilionid puts the secretion to
T Yagi et al.
Journal of bioenergetics and biomembranes, 8(5), 247-255 (1976-10-01)
The regulation by adenylates of activities of various partial electron transport systems in spinach chloroplasts was studied using systems from H2O to 2,5-dimethyl-p-benzoquinone, H2O to 2,6-dichlorophenolindophenol, reduced 2,6-dichlorophenolindophenol to methyl viologen, and H2O to methyl viologen or ferricyanide. Adenylates regulated
P Mäenpää et al.
Plant molecular biology, 38(6), 1191-1200 (1998-12-30)
Ala-251 in the membrane-parallel helix in the D-E loop of the D1 polypeptide close to the Q(B) pocket of photosystem II (PS II), was mutated to aspartate (D), lysine (K), leucine (L) or serine (S) in Synechocystis 6803. O2 evolution
J Cao et al.
Biochimica et biophysica acta, 1015(2), 180-188 (1990-02-02)
Upon illumination, a dark-adapted photosynthetic sample shows time-dependent changes in chlorophyll (Chl) a fluorescence yield, known as the Kautsky phenomenon or the OIDPS transient. Based on the differential effects of electron acceptors such as 2,5-dimethyl-p-benzoquinone (DMQ) and 2,6-dichloro-p-benzoquinone (DCBQ) on

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