Skip to Content
Merck
All Photos(4)

Documents

A88107

Sigma-Aldrich

p-Anisaldehyde

98%

Synonym(s):

p-Methoxybenzaldehyde, 4-Methoxybenzaldehyde, Aubépine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3OC6H4CHO
CAS Number:
Molecular Weight:
136.15
Beilstein:
471382
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.7 (vs air)

Quality Level

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)

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

Signal Word

Warning

Hazard Statements

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Articles

High-Performance Thin-Layer chromatography (HPTLC) quantification of methylglyoxal (MGO) in complex and matrix rich manuka honey offering quick sample preparation, high-matrix tolerance, and high-throughput.

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service