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Merck

B56501

Sigma-Aldrich

4-Bromanisol

≥99.0%

Synonym(e):

1-Brom-4-methoxy-benzol

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About This Item

Lineare Formel:
BrC6H4OCH3
CAS-Nummer:
Molekulargewicht:
187.03
Beilstein:
1237590
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

≥99.0%

Form

liquid

Brechungsindex

n20/D 1.564 (lit.)

bp

223 °C (lit.)

mp (Schmelzpunkt)

9-10 °C (lit.)

Dichte

1.494 g/mL at 25 °C (lit.)

SMILES String

COc1ccc(Br)cc1

InChI

1S/C7H7BrO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3

InChIKey

QJPJQTDYNZXKQF-UHFFFAOYSA-N

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Allgemeine Beschreibung

4-Bromoanisole is a useful brominating reagent. It is formed as reaction product in the reaction between HOBr and anisole. Suzuki coupling of 4-bromoanisole with phenylboronic acid catalyzed by palladium pincer complexes has been studied. Heck Reaction of 4-bromoanisole with ethyl acrylates in room-temperature ionic liquids is reported to afford ethyl 4-methoxycinnamate.

Anwendung

4-Bromoanisole was used in the synthesis of aryl 1,3-diketones.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral - Skin Irrit. 2

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

201.2 °F

Flammpunkt (°C)

94 °C

Persönliche Schutzausrüstung

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Reaction conditions for the three-component synthesis of aryl 1,3-diketones are reported applying the palladium-catalyzed carbonylative α-arylation of ketones with aryl bromides. The optimal conditions were found by using a catalytic system derived from [Pd(dba)2] (dba=dibenzylideneacetone) as the palladium source and
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Artikel

The Heck reaction is the palladium catalyzed cross-coupling reaction between alkenes and aryl or vinyl halides (or triflates) to afford substituted alkenes.

Global Trade Item Number

SKUGTIN
B56501-100G4061833434017
B56501-500G4061838352583
B56501-50G4061833434024

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