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195898

3-(4-Methoxyphenoxy)benzaldehyde

97%

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About This Item

Linear Formula:
CH3OC6H4OC6H4CHO
CAS Number:
62373-80-2
Molecular Weight:
228.24
NACRES:
NA.22
PubChem Substance ID:
24851722
UNSPSC Code:
12352100
EC Number:
263-527-7
MDL number:
MFCD00003358
Assay:
97%
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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

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

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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Certificates of Analysis (COA)

Lot/Batch Number
16021ER
12401HU
10830TA
07621BO

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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

Global Trade Item Number

SKUGTIN
195898-1G04061836683009