195898
3-(4-甲氧基苯氧基)苯甲醛
97%
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线性分子式:
CH3OC6H4OC6H4CHO
化学文摘社编号:
分子量:
228.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
263-527-7
MDL number:
产品名称
3-(4-甲氧基苯氧基)苯甲醛, 97%
InChI key
WLFDEVVCXPTAQA-UHFFFAOYSA-N
InChI
1S/C14H12O3/c1-16-12-5-7-13(8-6-12)17-14-4-2-3-11(9-14)10-15/h2-10H,1H3
SMILES string
COc1ccc(Oc2cccc(C=O)c2)cc1
assay
97%
refractive index
n20/D 1.596 (lit.)
bp
145 °C/0.4 mmHg (lit.)
density
1.089 g/mL at 25 °C (lit.)
functional group
aldehyde
Application
3-(4-Methoxyphenoxy)benzaldehyde was used as building block in the synthesis of tetrahydroisoquinolinones. It was used as internal standard during the determination of hydrolytic activity of pyrethroids by gas chromatography-mass spectrometry.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
法规信息
新产品
此项目有
Kosuke Nishi et al.
Archives of biochemistry and biophysics, 445(1), 115-123 (2005-12-20)
Carboxylesterases hydrolyze a large array of endogenous and exogenous ester-containing compounds, including pyrethroid insecticides. Herein, we report the specific activities and kinetic parameters of human carboxylesterase (hCE)-1 and hCE-2 using authentic pyrethroids and pyrethroid-like, fluorescent surrogates. Both hCE-1 and hCE-2
M Lebl
Bioorganic & medicinal chemistry letters, 9(9), 1305-1310 (1999-05-26)
A new technique for high throughput solid phase synthesis using the centrifuge based liquid removal from readily available standard microtiterplates is described. This technique eliminates the filtration step and is therefore applicable to simultaneous processing of an unlimited number of
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