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Merck

A88107

p-Anisaldehyde

98%

Synonym(s):

p-Methoxybenzaldehyde, 4-Methoxybenzaldehyde, Aubépine

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About This Item

Linear Formula:
CH3OC6H4CHO
CAS Number:
123-11-5
Molecular Weight:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891369
EC Number:
204-602-6
Beilstein/REAXYS Number:
471382
MDL number:
MFCD00003385

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Product Name

p-Anisaldehyde, 98%

InChI key

ZRSNZINYAWTAHE-UHFFFAOYSA-N

InChI

1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3

SMILES string

[H]C(=O)c1ccc(OC)cc1

vapor density

4.7 (vs air)

assay

98%

form

liquid

refractive index

n20/D 1.573 (lit.)

bp

248 °C (lit.)

mp

−1 °C (lit.)

density

1.119 g/mL at 25 °C (lit.)

Quality Level

200

Gene Information

human ... CYP1A2(1544)

Related Categories

Application

p-Anisaldehyde may be used as a triplet sensitizer to catalyze the photochemical intermolecular atom-transfer radical addition (ATRA) of haloalkanes onto olefins. It can be used to synthesize 2-(4-methoxybenzylidene)-N-(4-(N-(1-phenyl-1H-pyrazol-5-yl)sulfamoyl)phenyl) hydrazinecarbothioamide. It is also used as a stain for detecting non UV-active substances using thin layer chromatography (TLC).

pictograms

Health hazard
GHS08

signalword

Warning

Hazard Classifications

Aquatic Chronic 3 - Repr. 2

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

240.8 °F - closed cup

flash_point_c

116 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
0000526875
0000526875
SDBB7180
MKCZ7514
MKCZ4416

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Synthesis, structural characterization and anticancer evaluation of pyrazole derivatives.
El-Gaby MS
Medicinal Chemistry Research, 27(1), 72-79 (2018)
Photo?Organocatalysis of Atom?Transfer Radical Additions to Alkenes.
Arceo E
Angewandte Chemie (International Edition in English), 53(45), 12064-12068 (2014)
Qingyao Wu et al.
Nature communications, 12(1), 483-483 (2021-01-22)
Artificial photosynthesis of H2O2 from H2O and O2, as a spotless method, has aroused widespread interest. Up to date, most photocatalysts still suffer from serious salt-deactivated effects with huge consumption of photogenerated charges, which severely limit their wide application. Herein
Stereocontrolled cascade cyclisation of campholenic enol?ether derivatives: en route to vetiver?scented spiroxides.
Ondet P
European Journal of Organic Chemistry, (8), 980-989 (2018)
Guozhu Zhang et al.
Journal of the American Chemical Society, 130(38), 12598-12599 (2008-08-30)
A novel approach to generate Au-containing all-carbon 1,3-dipoles is developed via an unprecedented migration-fragmentation of ketals/acetals. These in situ generated dipoles undergo rapid [3+2] cycloaddition under mild conditions with various enones/enals, electron-rich aromatic aldehydes, and N-benzylindole, leading to flexible formation
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