CAS 50910-55-9
:2-Amino-3,5-dibromobenzaldeído
- 2-Amino-3,5-Dibromo-Benzaldehyde
- 3,5-Dibromo-2-aminobenzaldehyde
- 3,5-Dibromo-O-Aminobenzaldehyde
- Benzaldehyde, 2-amino-3,5-dibromo-
- 2-Amino-3,5-Bromo Benzaldehyde
- 2-Amino-3,5-dibromobenzaldehyde
2-Amino-3,5-dibromobenzaldehyde
CAS:Fórmula:C7H5Br2NOPureza:>98.0%(GC)Cor e Forma:Light yellow to Amber to Dark green powder to crystalPeso molecular:278.932-Amino-3,5-dibromobenzaldehyde, 97%
CAS: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 reference has not changed as a part of the brand transition to Thermo Sci
Fórmula:C7H5Br2NOPureza:97%Peso molecular:278.932-Amino-3,5-dibromobenzaldehyde
CAS:Fórmula:C7H5Br2NOPureza:97%Cor e Forma:SolidPeso molecular:278.9287BroMhexine IMpurity B
CAS:Bromhexine Impurity B reagent used in the preparation of Ambroxol and Bromhexine (B678600) metabolites Ambroxol EP Impurity E.Fórmula:C7H5Br2NOPureza:99.20%Cor e Forma:Light Yellow Crystal PowderPeso molecular:278.93Ambroxol EP Impurity E (Bromhexine EP Impurity B)
CAS:Fórmula:C7H5Br2NOCor e Forma:Pale Yellow SolidPeso molecular:278.932-Amino-3,5-dibromobenzaldehyde
CAS:2-Amino-3,5-dibromobenzaldehydePureza:98%Peso molecular:278.93g/mol2-Amino-3,5-dibromobenzaldehyde
CAS:Produto ControladoFórmula:C7H5Br2NOCor e Forma:NeatPeso molecular:278.932-Amino-3,5-dibromo-benzaldehyde
CAS:Produto ControladoImpurity Bromhexine EP Impurity B
Applications 2-Amino-3,5-dibromo-benzaldehyde (Bromhexine EP Impurity B) reagent used in the preparation of Ambroxol and Bromhexine (B678600) metabolites Ambroxol EP Impurity E..
References Fadeyi, O., et al.: Bioorg. Med. Chem. Lett., 18, 4172 (2008), Liu, J., et al.: J. Pharm. Biomed. Anal., 51, 1134 (2010),Fórmula:C7H5Br2NOCor e Forma:YellowPeso molecular:278.932-Amino-3,5-dibromobenzaldehyde
CAS:2-Amino-3,5-dibromobenzaldehyde (2ADB) is a tetradentate ligand that can be used to prepare pharmaceutical preparations. 2ADB has been shown to react with methyl anthranilate in the presence of nitrobenzene and hydrochloric acid, forming x-ray crystal structures. The reaction products were quinoline derivatives. 2ADB has an antiinflammatory activity and can be used as a potential drug for the treatment of arthritis.
Fórmula:C7H5Br2NOPureza:Min. 95%Cor e Forma:PowderPeso molecular:278.93 g/mol2-Amino-3,5-dibromobenzaldehyde
CAS:Fórmula:C7H5Br2NOPureza:98%Cor e Forma:Pale yellow to yellow green powderPeso molecular:278.931











