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线性分子式:
C10H7OCH3
化学文摘社编号:
分子量:
158.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-696-1
Beilstein/REAXYS Number:
774884
MDL number:
产品名称
1-甲氧基萘, ≥98%
InChI key
NQMUGNMMFTYOHK-UHFFFAOYSA-N
InChI
1S/C11H10O/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3
SMILES string
COc1cccc2ccccc12
assay
≥98%
form
liquid
refractive index
n20/D 1.621 (lit.)
bp
135-137 °C/12 mmHg (lit.)
density
1.09 g/mL at 25 °C (lit.)
Quality Level
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Application
1-Methoxynaphthalene was used to study the peroxygenase activity of CcP. It was also used to synthesize prenyl naphthalen-ols.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
Eyeshields, Gloves
James E Erman et al.
BMC biochemistry, 14, 19-19 (2013-07-31)
The cytochrome P450s are monooxygenases that insert oxygen functionalities into a wide variety of organic substrates with high selectivity. There is interest in developing efficient catalysts based on the "peroxide shunt" pathway in the cytochrome P450s, which uses H2O2 in
Kazutoshi Shindo et al.
Bioscience, biotechnology, and biochemistry, 75(3), 505-510 (2011-03-11)
We performed combinational bioconversion of substituted naphthalenes with PhnA1A2A3A4 (an aromatic dihydroxylating dioxygenase from marine bacterium Cycloclasticus sp. strain A5) and prenyltransferase NphB (geranyltransferase from Streptomyces sp. strain CL190) or SCO7190 (dimethylallyltransferase from Streptomyces coelicolor A3(2)) to produce prenyl naphthalen-ols.
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