51386
p-苯醌
pharmaceutical secondary standard; traceable to USP
别名:
醌
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线性分子式:
C6H4(=O)2
化学文摘社编号:
分子量:
108.09
EC Number:
203-405-2
UNSPSC Code:
12352005
PubChem Substance ID:
Beilstein/REAXYS Number:
773967
MDL number:
grade
certified reference material, pharmaceutical secondary standard
agency
traceable to USP 1056504
vapor density
3.73 (vs air)
vapor pressure
0.1 mmHg ( 25 °C)
autoignition temp.
815 °F
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
113-115 °C (lit.)
format
neat
storage temp.
2-8°C
SMILES string
O=C1C=CC(=O)C=C1
InChI
1S/C6H4O2/c7-5-1-2-6(8)4-3-5/h1-4H
InChI key
AZQWKYJCGOJGHM-UHFFFAOYSA-N
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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法规信息
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Rozbeh Baradaran et al.
Nature, 494(7438), 443-448 (2013-02-19)
Complex I is the first and largest enzyme of the respiratory chain and has a central role in cellular energy production through the coupling of NADH:ubiquinone electron transfer to proton translocation. It is also implicated in many common human neurodegenerative
Takafumi Hasegawa et al.
Journal of neurochemistry, 87(2), 470-475 (2003-09-27)
Oxidized metabolites of dopamine, known as dopamine quinone derivatives, are thought to play a pivotal role in the degeneration of dopaminergic neurons. Although such quinone derivatives are usually produced via the autoxidation of catecholamines, tyrosinase, which is a key enzyme
GuangRong Peh et al.
Organic letters, 14(21), 5614-5617 (2012-10-26)
Cyclopropane-substituted allylic ethers react with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone to form oxocarbenium ions with no competitive ring cleavage. This reaction can be used for the preparation of cyclopropane-substituted tetrahydropyrans. The protocol was used as a key step in the total synthesis of the