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195898

Sigma-Aldrich

3-(4-Methoxyphenoxy)benzaldehyde

97%

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Linear Formula:
CH3OC6H4OC6H4CHO
CAS Number:
62373-80-2
Molecular Weight:
228.24
EC Number:
263-527-7
MDL number:
MFCD00003358
PubChem Substance ID:
24851722
NACRES:
NA.22

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.)

SMILES string

COc1ccc(Oc2cccc(C=O)c2)cc1

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

InChI key

WLFDEVVCXPTAQA-UHFFFAOYSA-N

Related Categories

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 Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), 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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