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A88107

Sigma-Aldrich

p-Anisaldehyde

98%

Sinonimo/i:

p-Methoxybenzaldehyde, 4-Methoxybenzaldehyde, Aubépine

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About This Item

Formula condensata:
CH3OC6H4CHO
Numero CAS:
123-11-5
Peso molecolare:
136.15
Beilstein:
471382
Numero CE:
204-602-6
Numero MDL:
MFCD00003385
Codice UNSPSC:
12352100
ID PubChem:
24891369
NACRES:
NA.22

Densità del vapore

4.7 (vs air)

Saggio

98%

Stato

liquid

Indice di rifrazione

n20/D 1.573 (lit.)

P. ebollizione

248 °C (lit.)

Punto di fusione

−1 °C (lit.)

Densità

1.119 g/mL at 25 °C (lit.)

Stringa SMILE

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

InChI

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

Informazioni sul gene

human ... CYP1A2(1544)

Categorie correlate

Applicazioni

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).

Pittogrammi

Health hazard
GHS08

Avvertenze

Warning

Indicazioni di pericolo

H361fd,H412

Classi di pericolo

Aquatic Chronic 3 - Repr. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

240.8 °F - closed cup

Punto d’infiammabilità (°C)

116 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
0000143956
MKCQ6292
MKCQ5437
0000135724
0000135303

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m-Anisaldehyde 97%

Sigma-Aldrich

129658

m-Anisaldehyde

2-Methoxybenzaldehyde 98%

Sigma-Aldrich

109622

2-Methoxybenzaldehyde

Trimethyl phosphonoacetate 98%

Sigma-Aldrich

T79758

Trimethyl phosphonoacetate

o-Anisaldehyde ≥97%, FG

Sigma-Aldrich

W407701

o-Anisaldehyde

4-Chlorobenzaldehyde 97%

Sigma-Aldrich

112216

4-Chlorobenzaldehyde

p-Tolualdehyde ≥97%, FG

Sigma-Aldrich

W306800

p-Tolualdehyde

4-Nitrobenzaldehyde 98% (GC)

Sigma-Aldrich

130176

4-Nitrobenzaldehyde

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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