70430
1,4-二羟基萘
technical, ≥90% (HPLC)
别名:
1,4-二氧萘酚, 对-萘并氢醌 (α)
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关于此项目
经验公式（希尔记法）:
C10H8O2
化学文摘社编号:
分子量:
160.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-336-4
Beilstein/REAXYS Number:
1307689
MDL number:
Assay:
≥90% (HPLC)
Form:
crystals
产品名称
1,4-二羟基萘, technical, ≥90% (HPLC)
InChI
1S/C10H8O2/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6,11-12H
InChI key
PCILLCXFKWDRMK-UHFFFAOYSA-N
SMILES string
Oc1ccc(O)c2ccccc12
grade
technical
assay
≥90% (HPLC)
form
crystals
mp
191-192 °C (dec.)
Quality Level
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Autoxidation of naphthohydroquinones: effects of metals, chelating agents, and superoxide dismutase.
R Munday
Free radical biology & medicine, 22(4), 689-695 (1997-01-01)
At neutral pH, 1,4-naphthohydroquinone and 2-methyl-1,4-naphthohydroquinone readily autoxidize to the corresponding quinones. In an unpurified phosphate buffer, the autoxidation of both substances proceeded in a linear fashion after a brief lag phase. Addition of a chelating agent or purification of
R Munday
Free radical research, 32(3), 245-253 (2000-03-24)
The rates of autoxidation of a number of pure naphthohydroquinones have been determined, and the effects of pH, superoxide dismutase (SOD) and of the parent naphthoquinone on the oxidation rates have been investigated. Most compounds were slowly oxidised in acid
Selective nonpeptidic inhibitors of herpes simplex virus type 1 and human cytomegalovirus proteases.
M Matsumoto et al.
Biological & pharmaceutical bulletin, 24(3), 236-241 (2001-03-21)
The proteases encoded by herpesviruses including herpes simplex virus type 1 (HSV-1) and human cytomegalovirus (HCMV) are attractive targets for antiviral drug development because of their important roles in viral replication. We randomly screened a chemical compound library for inhibitory
María Teresa Molina et al.
The Journal of organic chemistry, 74(24), 9573-9575 (2009-11-27)
The NHC-catalyzed conjugate hydroacylation of 1,4-naphthoquinones allows for the synthesis of monoacylated 1,4-dihydroxynaphthalene derivatives. These targets, difficult to prepare selectively by standard protocols, represent important intermediates in the elaboration of highly substituted 1,4-naphthoquinone derivatives, which constitute relevant pharmaceutical scaffolds. High
Kevin W Wellington et al.
Bioorganic & medicinal chemistry, 20(14), 4472-4481 (2012-06-12)
Nuclear monoamination of a 1,4-naphthohydroquinone with primary aromatic amines was catalysed by the commercial laccase, Novozym 51003, from Novozymes to afford aminonaphthoquinones. The synthesis was accomplished by reacting a mixture of the primary amine and 1,4-naphthohydroquinone in succinate-lactate buffer and
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