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72824-04-5 - Allylboronic acid pinacol ester, 98+% - 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane - L16232 - Alfa Aesar

L16232 Allylboronic acid pinacol ester, 98+%

Codice CAS
72824-04-5
Sinonimi
2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Dimensioni Prezzo ($) Quantità Disponibilità
1g 33,10
5g 116,00
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Allylboronic acid pinacol ester, 98+%

MDL
MFCD00013347

Proprietà chimiche

Formula
C9H17BO2
Peso formula
168.05
Punto di ebollizione
50-53°/5mm
Punto di infiammabilità
46°(140°F)
Densità
0.890
Indice di rifrazione
1.4270
Solubilità
Not miscible or difficult to mix in water.

Applicazioni

Allylboronic acid pinacol ester reacts with carboxylic acids, in the presence of tri-n-butyltin hydride, to give homoallylic alcohols in good yield. Homoallylic alcohols can also be formed by allylboration of aldehydes. It is a reagent used for palladium-catalyzed Suzuki-Miyaura cross-coupling reactions and olefin metathesis, intermolecular radical additions, allylboration of aldehydes catalyzed by chiral spirobiindane diol (SPINOL) based phosphoric acids, cobalt-catalyzed regioselective hydrovinylation of dienes with alkenes, nucleic acid-templated energy transfer leading to a photorelease reaction and stereoselective indium-catalyzed Hosomi-Sakurai reactions.

Note

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Recommended storage temperature is 2 - 8°C. Store under inert gas. It is sensitive to moisture. Incompatible with oxidizing agents.

Letteratura

Sambasivarao Kotha.; Arjun S Chavan.; Mobin Shaikh. Diversity-oriented approach to macrocyclic cyclophane derivatives by Suzuki-Miyaura cross-coupling and olefin metathesis as key steps. Journal of Organic Chemistry. 2012, 77 (1), 482-489.

Nicolas Charrier, Zhibo Liu, Samir Z Zard. Desulfonylative radical ring closure onto aromatics. A modular route to benzazepin-2-ones and 5-arylpiperidin-2-ones. Organic Letters. 2012, 14 (8), 2018-2021.

Reacts with carboxylic acids, in the presence of tri-n-butyltin hydride, to give homoallylic alcohols in good yield: Synthesis, 1573 (2001):

Homoallylic alcohols can also be formed by allylboration of aldehydes; the reaction has been found to be accelerated by Lewis acids, e.g. AlCl3 or Sc(OTf)3: J. Am. Chem. Soc., 124, 12414 (2002).

Rischio GHS e dichiarazioni precauzionali

Dichiarazioni di rischio (UE): H226

Flammable liquid and vapour.

Dichiarazioni precauzionali: P260-P201-P280a-P304+P340-P405-P501a

Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves and eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Altri riferimenti

Beilstein
4244068
Classe di rischio
3
Gruppo di imballaggio
III
Codice tariffe armonizzato
2934.99
TSCA
No

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