Phenylselenyl bromide

Synonym: Benzeneselenenyl bromide; Benzeneselenyl bromide
Molecular Formula: C6H5SeBr
Molecular Weight: 235.97
CAS Number: 34837-55-3
MDL number: MFCD00000047
EC Number: 252-238-1
Note: Prices are for comparison only. Contact Sales for current pricing.
Purity: 98 %
Packing size: 5 G  
Form: solid  
52.50 EUR
Purity: 98 %
Packing size: 25 G  
Form: solid  
153.30 EUR



Safety Information


Hazard Statements

H373
H301
H410
H331
H400
H290
H301 + H331

Precautionary Statements

P301 + P310
P304 + P340 + P311
P264
P270
P501
P273
P261
P271
P391
P405
P260
P314
P403 + P233
P234
P390
P304 + P340
P330
P321
P319
P301 + P316
P316

Pictograms

 Product Description

Phenylselenyl bromide is an organoselenium compound used in organic synthesis. It features a phenyl group bonded to selenium and bromine, making it reactive in various chemical reactions.

 

Application:

Phenylselenyl bromide is used as a reagent in organic synthesis, particularly for introducing selenium into molecules and facilitating oxidative reactions.

 

 

Articles:

- Regiodivergent metal-catalyzed B(4)- and C(1)-selenylation of o-carboranes

Publication Date: 3rd December 2022

Kyungsup Lee, Jordan L. Harper, Tae Hyeon Kim, Hee Chan Noh, Dongwook Kim, Paul Ha-Yeon Cheong and Phil Ho Lee

https://doi.org/10.1039/D2SC05590B

 

- Electrophile-induced generation of cyclic azomethine imines from steroidal δ-alkenyl hydrazones

Publication Date: Available online 13 January 2009

Erzsébet Mernyák, László Márk, Éva Frank, Gyula Schneider, János Wölfling

https://doi.org/10.1016/j.steroids.2009.01.001

 

- X=Y–ZH Systems as potential 1,3-dipoles. Part 54: Stereo- and facially-selective formation of bridged bicyclic N-heterocycles via a sequential one-pot electrophile induced oxime→nitrone→cycloaddition sequence. Multiplication of chirality

Publication Date: Available online 13 June 2002

H Ali Dondas, Ronald Grigg, Sylvie Thibault, W Anthony Thomas, Mark Thornton-Pett

https://doi.org/10.1016/S0040-4020(02)00564-1