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A88107

Sigma-Aldrich

p-anisaldéhyde

98%

Synonyme(s) :

4-méthoxybenzaldéhyde

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About This Item

Formule linéaire :
CH3OC6H4CHO
Numéro CAS:
123-11-5
Poids moléculaire :
136.15
Numéro Beilstein :
471382
Numéro CE :
204-602-6
Numéro MDL:
MFCD00003385
Code UNSPSC :
12352100
ID de substance PubChem :
24891369
Nomenclature NACRES :
NA.22

Densité de vapeur

4.7 (vs air)

Niveau de qualité

200

Pureté

98%

Forme

liquid

Indice de réfraction

n20/D 1.573 (lit.)

Point d'ébullition

248 °C (lit.)

Pf

−1 °C (lit.)

Densité

1.119 g/mL at 25 °C (lit.)

Chaîne SMILES 

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

InChI

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

Clé InChI

ZRSNZINYAWTAHE-UHFFFAOYSA-N

Informations sur le gène

human ... CYP1A2(1544)

Catégories apparentées

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).

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Warning

Mentions de danger

H361fd,H412

Classification des risques

Aquatic Chronic 3 - Repr. 2

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

240.8 °F - closed cup

Point d'éclair (°C)

116 °C - closed cup

Équipement de protection individuelle

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

Certificats d'analyse (COA)

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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
Photo?Organocatalysis of Atom?Transfer Radical Additions to Alkenes.
Arceo E
Angewandte Chemie (International Edition in English), 53(45), 12064-12068 (2014)
Synthesis, structural characterization and anticancer evaluation of pyrazole derivatives.
El-Gaby MS
Medicinal Chemistry Research, 27(1), 72-79 (2018)
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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