4-[(Trimethylsilyl)ethynyl]benzaldehyde, 97%

Name: 4-[(Trimethylsilyl)ethynyl]benzaldehyde, 97%
SKU: H55060.03

CAS: 77123-57-0 | C12H14OSi | 202.33 g/mol

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数量:

1 g

5 g

25 g

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製品番号（カタログ番号） H55060.03

または、製品番号H55060-03

価格（JPY）

数量:

1 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

CAS77123-57-0

IUPAC Name4-[2-(trimethylsilyl)ethynyl]benzaldehyde

Molecular FormulaC12H14OSi

InChI KeyUZQDUXAJFTWMDT-UHFFFAOYSA-N

SMILESC[Si](C)(C)C#CC1=CC=C(C=O)C=C1

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仕様

スペックシート

Assay (GC)>96.0%

It is an important raw material and intermediate used in organic synthesis, Pharmaceuticals, agrochemicals and dyestuffs.

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
It is an important raw material and intermediate used in organic synthesis, Pharmaceuticals, agrochemicals and dyestuffs.

Notes
Store at 4°C. Keep away from oxidizing agents.

RUO – Research Use Only

General References:

William B. Austin.; Norman Bilow.; William J. Kelleghan.; Kreisler S. Y. Lau. Facile synthesis of ethynylated benzoic acid derivatives and aromatic compounds via ethynyltrimethylsilane. J. Org. Chem. 1981, 46 (11), 2280-2286.
Aidan R. McDonald.; Nicole Franssen.; Gerard P.M. van Klink.; Gerard van Koten. Click’ silica immobilisation of metallo-porphyrin complexes and their application in epoxidation catalysis.J. Organomet. Chem. 2009, 694 (14),2153-2162.