CAS 29334-16-5
:4-Bromo-α-fenilbenzenometanol
- (4-Bromophenyl)(Phenyl)Methanol
- (4-Bromophenyl)phenylmethanol
- (R)-(4-bromophenyl)(phenyl)methanol
- (p-Bromophenyl)-α-phenylmethanol
- 4-(1-Hydroxybenzyl)bromobenzene
- 4-Bromo-α-phenylbenzenemethanol
- 4-Bromobenzhydrol
- Benzenemethanol, 4-bromo-α-phenyl-
- Benzhydrol, 4-bromo-
- Benzohydrol, 4-bromo-
- NSC 89817
- p-Bromobenzhydrol
- α-(4-Bromophenyl)benzenemethanol
- α-Phenyl-p-bromobenzyl alcohol
- Ver mais sinónimos
4-Bromobenzhydrol
CAS:Fórmula:C13H11BrOPureza:>97.0%(GC)Cor e Forma:White to Light yellow to Light orange powder to crystalPeso molecular:263.13Benzenemethanol, 4-bromo-α-phenyl-
CAS:Fórmula:C13H11BrOPureza:95%Cor e Forma:SolidPeso molecular:263.12984-Bromo-Alpha-phenylbenzenemethanol
CAS:Produto ControladoApplications 4-Bromo-α-phenylbenzenemethanol is used in the synthesis of diarylmethylpiperazines as potent and selective nonpeptidic δ-opioid receptor agonists. Is used in the ysnthesis of bronsted acid-catalyzed benzylation of 1,3-dicarbonyl derivatives.
References Plobeck, N. et al.: J. Med. Chem., 43, 3878 (2000); Sanz, R. et al.: Org. Lett., 9, 2027 (2007);Fórmula:C13H11BrOCor e Forma:NeatPeso molecular:263.134-Bromobenzhydrol
CAS:4-Bromobenzhydrol is a potent inhibitor of the enzyme histamine N-methyltransferase that is used in the treatment of chronic inflammatory disorders. In pharmacological tests, 4-bromobenzhydrol has been shown to be an inhibitor of acidic aldehyde reactions and also inhibits hypophosphorous acid formation. This drug also reacts with serum albumin, ethanolamine, and ethylene oxide to form a model protein. 4-Bromobenzhydrol has been shown to have immunosuppressive activity by inhibiting the T cell response.
Fórmula:C13H11BrOPureza:Min. 95%Cor e Forma:PowderPeso molecular:263.13 g/molRef: 3D-FB70740
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