CAS 6627-55-0
:2-Bromo-4-méthylphénol
- 2-Bromo-4-cresol
- 2-Bromo-p-cresol
- 2-Bromo-p-cresol (OH=1)
- 3-Bromo-4-Hydroxytoluene
- NSC 60115
- Phenol, 2-bromo-4-methyl-
- p-Cresol, 2-bromo-
- 2-Bromo-4-methylphenol
2-Bromo-4-methylphenol, 97%
CAS :It is applied as a compound responsible for iodine off-flavor in wines. 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 r
Formule :C7H7BrODegré de pureté :97%Couleur et forme :Liquid, Clear colorless to yellowMasse moléculaire :187.042-Bromo-4-methylphenol
CAS :Formule :C7H7BrODegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :187.0339Ref: IN-DA003GON
5g21,00€10g25,00€1kg271,00€25g28,00€50g53,00€5kgÀ demander100g62,00€10kgÀ demander250g120,00€25kgÀ demander500g208,00€2-Bromo-4-methylphenol
CAS :2-Bromo-4-methylphenolFormule :C7H7BrODegré de pureté :97%Couleur et forme : clear. almost colourless liquidMasse moléculaire :187.03g/mol2-Bromo-p-cresol
CAS :Formule :C7H7BrODegré de pureté :>98.0%(GC)Couleur et forme :White or Colorless to Light yellow powder to lump to clear liquidMasse moléculaire :187.042-Bromo-4-methylphenol
CAS :Produit contrôléApplications 2-Bromo-4-methylphenol is a useful synthetic intermediate. It was used in the synthesis of furan-2-ylmethylene thiazolidinediones as potent, and selective inhibitors of phosphoinositide 3-kinase γ. It was also a reactant used to prepare phosphoramidate and phosphorothioamidate analogs of amiprophos Me as potential antimalarial agents.
References Pomel, V., et al.: J. Med. Chem., 49, 3857 (2006); Mara, C., et al.: Bioorg. Med. Chem. Lett., 21, 6180 (2011)Formule :C7H7BrOCouleur et forme :NeatMasse moléculaire :187.032-Bromo-4-methylphenol
CAS :Formule :C7H7BrODegré de pureté :95%Couleur et forme :ClearMasse moléculaire :187.0362-Bromo-4-methylphenol
CAS :2-Bromo-4-methylphenol is an organic compound that has interactive effects with hydrochloric acid, molybdenum, and trifluoromethanesulfonic acid. It is soluble in water vapor, but insoluble in polyvinyl. 2-Bromo-4-methylphenol reacts with sodium hydroxide solution to form a hydroxide solution and sodium carbonate. The reaction product of 2-bromo-4-methylphenol with triterpenoid saponin produces fatty acids. This reaction occurs because the hydroxide ion from the sodium hydroxide solution attacks the ester group of the saponin, forming an alcohol group on one end and a carboxylic acid group on the other end. The benzyl groups are removed by hydrogenation to produce phenol.
Formule :C7H7BrODegré de pureté :Min. 95%Masse moléculaire :187.03 g/mol






