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Merck

A88107

Sigma-Aldrich

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
Beilstein:
471382
EC Number:
204-602-6
MDL number:
MFCD00003385
UNSPSC Code:
12352100
PubChem Substance ID:
24891369
NACRES:
NA.22

Key Documents

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vapor density

4.7 (vs air)

Quality Level

200

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.)

SMILES string

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

InChI

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

InChI key

ZRSNZINYAWTAHE-UHFFFAOYSA-N

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

Signal Word

Warning

Hazard Statements

H361fd,H412

Hazard Classifications

Aquatic Chronic 3 - Repr. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

240.8 °F - closed cup

Flash Point(C)

116 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000143956
MKCQ6292
MKCQ5437
0000135724
0000135303

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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)
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)
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
N Juillet et al.
Plant biology (Stuttgart, Germany), 13(4), 570-575 (2011-06-15)
It has often been proposed that nectarless deceptive orchid species exploit naïve pollinators in search of food before they learn to avoid their flowers, and that intraspecific floral trait polymorphism, often noted in this plant group, could prolong the time
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