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Merck
CN

154571

1-甲氧基萘

≥98%

别名:

1-萘甲醚

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关于此项目

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:
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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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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