CAS 50910-55-9

2-Amino-3,5-dibromobenzaldehyde

Description:

2-Amino-3,5-dibromobenzaldehyde is an organic compound characterized by the presence of an amino group, two bromine substituents, and an aldehyde functional group attached to a benzene ring. Its molecular structure features a benzaldehyde moiety, which contributes to its reactivity and potential applications in organic synthesis. The amino group (-NH2) enhances its solubility in polar solvents and can participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions. The bromine atoms, being electronegative, influence the compound's reactivity and can serve as leaving groups in certain reactions. This compound is typically used in the synthesis of more complex organic molecules and may exhibit biological activity, making it of interest in medicinal chemistry. Its physical properties, such as melting point and solubility, can vary based on the specific conditions and purity of the sample. As with many brominated compounds, it is essential to handle 2-amino-3,5-dibromobenzaldehyde with care due to potential toxicity and environmental concerns associated with brominated organic compounds.

Formula: C₇H₅Br₂NO

InChI: InChI=1S/C7H5Br2NO/c8-5-1-4(3-11)7(10)6(9)2-5/h1-3H,10H2

InChI key: InChIKey=RCPAZWISSAVDEA-UHFFFAOYSA-N

SMILES: C(=O)C1=C(N)C(Br)=CC(Br)=C1

Synonyms:

• 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: 50910-55-9

Formula: C₇H₅Br₂NO

Purity: >98.0%(GC)

Color and Shape: Light yellow to Amber to Dark green powder to crystal

Molecular weight: 278.93

Ref: 3B-D2625

2-Amino-3,5-dibromobenzaldehyde, 97%

CAS: 50910-55-9

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

Formula: C₇H₅Br₂NO

Purity: 97%

Molecular weight: 278.93

Ref: 02-H56015

2-Amino-3,5-dibromobenzaldehyde

CAS: 50910-55-9

Formula: C₇H₅Br₂NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 278.9287

Ref: IN-DA00329F

BroMhexine IMpurity B

CAS: 50910-55-9

Bromhexine Impurity B reagent used in the preparation of Ambroxol and Bromhexine (B678600) metabolites Ambroxol EP Impurity E.

Formula: C₇H₅Br₂NO

Purity: 99.20%

Color and Shape: Light Yellow Crystal Powder

Molecular weight: 278.93

Ref: TM-T1690

Ambroxol EP Impurity E (Bromhexine EP Impurity B)

CAS: 50910-55-9

Formula: C₇H₅Br₂NO

Color and Shape: Pale Yellow Solid

Molecular weight: 278.93

Ref: 4Z-A-606

2-Amino-3,5-dibromobenzaldehyde

CAS: 50910-55-9

2-Amino-3,5-dibromobenzaldehyde

Purity: 98%

Molecular weight: 278.93g/mol

Ref: 54-OR322519

BroMhexine IMpurity B

CAS: 50910-55-9

BroMhexine IMpurity B

Purity: ≥98%

Molecular weight: 278.93g/mol

Ref: 54-BUP19261

2-Amino-3,5-dibromobenzaldehyde

CAS: 50910-55-9

Formula: C₇H₅Br₂NO

Molecular weight: 278.93

Ref: 7W-GK7315

2-Amino-3,5-dibromobenzaldehyde

Controlled Product

CAS: 50910-55-9

Formula: C₇H₅Br₂NO

Color and Shape: Neat

Molecular weight: 278.93

Ref: 86-MM0005.02

2-Amino-3,5-dibromo-benzaldehyde

Controlled Product

CAS: 50910-55-9

Impurity 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),

Formula: C₇H₅Br₂NO

Color and Shape: Yellow

Molecular weight: 278.93

Ref: TR-A604610

Ambroxol EP Impurity E

CAS: 50910-55-9

Formula: C₇H₅Br₂NO

Molecular weight: 278.93

Ref: ST-EA-CP-A38005

2-Amino-3,5-dibromobenzaldehyde

CAS: 50910-55-9

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.

Formula: C₇H₅Br₂NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 278.93 g/mol

Ref: 3D-FA14503

2-Amino-3,5-dibromobenzaldehyde

CAS: 50910-55-9

Formula: C₇H₅Br₂NO

Purity: 98%

Color and Shape: Pale yellow to yellow green powder

Molecular weight: 278.931

Ref: 10-F212723