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Key Documents

Altri documenti

139726

Sigma-Aldrich

Benzoyl bromide

97%

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About This Item

Formula condensata:
C6H5COBr
Numero CAS:
618-32-6
Peso molecolare:
185.02
Beilstein:
1855439
Numero CE:
210-544-2
Numero MDL:
MFCD00000112
Codice UNSPSC:
12352100
ID PubChem:
24848428
NACRES:
NA.22

Livello qualitativo

200

Saggio

97%

Indice di rifrazione

n20/D 1.589 (lit.)

P. eboll.

218-219 °C (lit.)

Densità

1.57 g/mL at 25 °C (lit.)

Stringa SMILE

BrC(=O)c1ccccc1

InChI

1S/C7H5BrO/c8-7(9)6-4-2-1-3-5-6/h1-5H
AQIHMSVIAGNIDM-UHFFFAOYSA-N

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Descrizione generale

Benzoyl bromide is a versatile reagent which causes the benzoylation of ethers.

Applicazioni

Benzoyl bromide was used to study the kinetics of solvolysis of benzoyl halides in microemulsions of sodium bis(2-ethylhexyl)sulfosuccinate/isooctane/water at 25°C.

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H314,H335

Classi di pericolo

Skin Corr. 1B - STOT SE 3

Organi bersaglio

Respiratory system

Rischi supp

EUH014

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

194.0 °F - closed cup

Punto d’infiammabilità (°C)

90 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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L García-Río et al.
Langmuir : the ACS journal of surfaces and colloids, 22(18), 7499-7506 (2006-08-23)
A study was carried out on the solvolysis reactions of different benzoyl halides in microemulsions of water/NH4DEHP/isooctane, where NH4DEHP is ammonium bis(2-ethylhexyl) phosphate. Because of the low solubility of benzoyl halides in water, they are distributed between the continuous medium
Tülay Polat et al.
Carbohydrate research, 338(5), 447-449 (2003-02-01)
A simple and efficient method is developed for the chemoselective one-pot conversion of ethers (benzyl, TBDMS and acetal) to the corresponding benzoates by zinc triflate-catalyzed deprotection and benzoylation by benzoyl bromide. In the same reaction, methyl or p-methoxyphenyl glycosides are
Mai Do et al.
Nanoscale, 11(37), 17262-17269 (2019-06-28)
Perovskite nanoparticles have attracted the attention of research groups around the world for their impressive photophysical properties, facile synthesis and versatile surface chemistry. Here, we report a synthetic route that takes advantage of a suite of soluble precursors to generate
Dmitry Baranov et al.
ACS nano, 15(1), 650-664 (2020-12-23)
Excitonic coupling, electronic coupling, and cooperative interactions in self-assembled lead halide perovskite nanocrystals were reported to give rise to a red-shifted collective emission peak with accelerated dynamics. Here we report that similar spectroscopic features could appear as a result of

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