195898
3-(4-Methoxyphenoxy)benzaldehyde
97%
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About This Item
Linear Formula:
CH3OC6H4OC6H4CHO
CAS Number:
Molecular Weight:
228.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
263-527-7
MDL number:
Assay:
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.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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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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