Cinnamyl bromide, predominantly trans, 95%

Name: Cinnamyl bromide, predominantly trans, 95%
SKU: L01420.22

CAS: 4392-24-9 | C9H9Br | 197.075 g/mol

テクニカルサポートオーダーサポート

表示を変更

数量:

5 g

25 g

100 g

Chem dex^TM Webアプリをお試しください

製品番号（カタログ番号） L01420.22

または、製品番号L01420-22

価格（JPY）

数量:

100 g

一括またはカスタム形式をリクエストする

化学物質識別子

CAS4392-24-9

IUPAC Name[(1E)-3-bromoprop-1-en-1-yl]benzene

Molecular FormulaC9H9Br

InChI KeyRUROFEVDCUGKHD-QPJJXVBHSA-N

SMILESBrC\C=C\C1=CC=CC=C1

さらに表示

仕様

スペックシート

FormCrystals or powder or crystalline powder or fused solid or clear liquid as melt

Appearance (Color)White to pale cream to cream to yellow to orange to dark brown to brown

Assay (GC)≥94.0%

Refractive Index1.6160-1.6220 @ 20?C

Cinnamyl bromide, is used in the synthesis of naftifine.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Cinnamyl bromide, is used in the synthesis of naftifine.

Solubility
Soluble in methanol. Insoluble in water.

Notes
Light Sensitive. Keep container tightly closed. Store away from oxidizing agents.

RUO – Research Use Only

General References:

C.B. Kanner.; U.K. Pandit. Functionalized enamines—XXXII: Reaction of β-amino-α, β-unsaturated esters and amides with benzyl and cinnamyl bromides. Tetrahedron. 1982, 38, (24), 3597-3604.
Methvin B.Isaac.; Tak-Hang Chan. Indium mediated coupling of aldehydes with allyl bromides in aqueous media. the issue of regio- and diastereo-selectivity. Tetrahedron Letters. 1995, 36, (49), 8957-8960.