CAS 34837-55-3
:Bromure de benzeneselenenyle
- Benzeneselenenyl Bromide
- Benzeneselenyl bromide
- Phenylselenenyl bromide
- Phenylselenium bromide
- Phenylselenyl bromide
- Bromoselenobenzene
Phenylselenenyl bromide, 98%
CAS :Employed in the synthesis of enones by selenenylation of -cyano ketones with lithium naphthalenide. Phenylselenyl bromide was used in the preparation of exo-2-methyl-7-phenylselenyl-octahydro-8-oxa-2,7b-diaza-dicyclopenta[a,e]pentalene-1,3-dione and endo-2-methyl-7-phenylselanyl-octahydro-8-oxa-2,7b
Formule :C6H5BrSeDegré de pureté :98%Couleur et forme :Dark purple, Crystals or powder or crystalline powder or fused solidMasse moléculaire :235.98Phenyl Hypobromoselenoite
CAS :Phenyl HypobromoselenoiteDegré de pureté :98%Masse moléculaire :235.97g/molPhenylselenenyl Bromide
CAS :Formule :C6H5BrSeDegré de pureté :>97.0%(T)Couleur et forme :Orange to Brown to Dark purple powder to crystalMasse moléculaire :235.97Phenylselenyl Bromide
CAS :Produit contrôléApplications Phenylselenyl Bromide is used as a reagent in the synthesis of the antihyperglycemic agent, (+)-Antroquinonol. Phenylselenyl Bromide is also used in the preparation of 9-epi-Artemisinin (A777505); the chiral isomer of Artemisinin (A777500) which is an antimalarial.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Sulake, R.S., et al.: J. Org. Chem., 80, 6044 (2015); Orabi, K.Y. et al.: Phytochem., 51, 257 (1999); Jefford, C.W. et al.: Helv. Chim. Acta, 83, 1239 (2000); Klayman, D.L., et al.: Science, 228, 1049 (1985)Formule :C6H6BrSeCouleur et forme :NeatMasse moléculaire :236.976Phenylselenenyl bromide
CAS :Phenylselenenyl bromide is a fatty acid with a selenium atom in the side chain. It has an unsymmetrical structure and reacts with thrombin receptor, leading to the activation of protein C. Phenylselenenyl bromide is also converted to a glucuronide conjugate in the liver. This compound can be used as an immunosuppressant and has been shown to have anti-inflammatory effects in animal models of autoimmune diseases. Phenylselenenyl bromide may also inhibit nitric oxide production by reacting with nitro groups.br> Phenylselenenyl bromide contains nitrogen atoms that are asymmetric because they are not paired together. This means that one of the two nitrogen atoms is surrounded by four different substituents, while the other nitrogen atom is only surrounded by three different substituents. The structure of phenylselenenynl bromide makes it difficult
Formule :C6H5BrSeDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :235.97 g/molPhenylselenyl bromide
CAS :Formule :C6H5BrSeDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :235.9679






