CAS 64591-03-3

Formula: C3H2Br2N2

InChI: InChI=1S/C3H2Br2N2/c4-2-1-6-3(5)7-2/h1H,(H,6,7)

InChI key: KJBTZMYWBSAZAQ-UHFFFAOYSA-N

SMILES: C1=C(NC(=N1)Br)Br

2,5-Dibromo-1H-imidazole

CAS: 64591-03-3

Formula: C₃H₂Br₂N₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 225.8694

Ref: IN-DA0038KB

2,4-Dibromo-1H-imidazole

CAS: 64591-03-3

2,4-Dibromo-1H-imidazole

Formula: C₃H₂Br₂N₂

Purity: 97%

Color and Shape: Solid-Powder

Molecular weight: 225.86937

Ref: 54-OR1229

2,4-Dibromo-1H-imidazole

CAS: 64591-03-3

Formula: C₃H₂Br₂N₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 225.871

Ref: 10-F211244

2,5-Dibromo-1H-imidazole

CAS: 64591-03-3

2,5-Dibromo-1H-imidazole

Formula: C₃H₂Br₂N₂

Purity: 98%

Molecular weight: 225.87

Ref: IN-DG66598

2,4-Dibromo-1H-imidazole

CAS: 64591-03-3

2,4-Dibromo-1H-imidazole is a boronate. It is used in the synthesis of heterocyclic compounds. In this process, 2,4-dibromo-1H-imidazole reacts with an alkyl or aryl halide to form a boronic acid that can be coupled with other molecules to form new products. The boronic acids made from 2,4-dibromo-1H-imidazole are versatile intermediates for organic synthesis and can be used as starting materials for the preparation of pharmaceuticals and other useful substances. 2,4-Dibromo-1H-imidazole is also used in Suzuki reactions to form carbon–carbon bonds. This reaction uses palladium as a catalyst to generate new carbon–carbon bonds between two different organic molecules.

Formula: C₃H₂Br₂N₂

Purity: Min. 95%

Molecular weight: 225.87 g/mol

Ref: 3D-FD155723