Description

6-Bromonicotinamide (CAS No. 889676-37-3) is a high-purity brominated pyridine derivative with the molecular formula C₆H₅BrN₂O. This compound, also known as 6-bromopyridine-3-carboxamide, is a versatile intermediate in organic synthesis and pharmaceutical research. Its unique structure, featuring a bromine substituent at the 6-position and a carboxamide group at the 3-position of the pyridine ring, makes it a valuable building block for the development of novel heterocyclic compounds.

Our 6-Bromonicotinamide is rigorously tested to ensure superior quality, with purity levels exceeding 98% (HPLC). It is supplied as a fine white to off-white crystalline powder, packaged under inert conditions to guarantee stability and longevity. Suitable for a wide range of applications, including medicinal chemistry, agrochemical research, and material science, this compound is an essential reagent for researchers seeking to explore the reactivity of halogenated nicotinamide derivatives.

Key Features:

• CAS No.: 889676-37-3
• Molecular Weight: 201.02 g/mol
• Synonyms: 6-Bromopyridine-3-carboxamide, MFCD00266840
• Storage: Store at 2-8°C in a dry, well-ventilated area
• Hazard Codes: H302, H315, H319, H335

Properties

• CAS Number: 889676-37-3
• Complexity: 140
• IUPAC Name: 6-bromopyridine-3-carboxamide
• InChI: InChI=1S/C6H5BrN2O/c7-5-2-1-4(3-9-5)6(8)10/h1-3H,(H2,8,10)
• InChI Key: SNMZXTXZEQGKBG-UHFFFAOYSA-N
• Exact Mass: 199.95853
• Molecular Formula: C6H5BrN2O
• Molecular Weight: 201.02
• SMILES: C1=CC(=NC=C1C(=O)N)Br
• Topological: 56
• Monoisotopic Mass: 199.95853
• Synonyms: 6-Bromonicotinamide, 889676-37-3, 6-bromopyridine-3-carboxamide, MFCD00266840, 3-Pyridinecarboxamide,6-bromo-, 6-Bromo-nicotinamide, SCHEMBL668418, SCHEMBL22229965, DTXSID90593592, SNMZXTXZEQGKBG-UHFFFAOYSA-N, AKOS009456291, DS-2361, MB01098, PS-4878, SY047606, CS-0044657, O11563

Application

6-Bromonicotinamide serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules targeting neurological and metabolic disorders. Its bromine moiety facilitates cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, enabling the construction of complex heterocyclic scaffolds. Researchers also utilize this compound in agrochemical studies to develop novel pesticides and herbicides. Additionally, its carboxamide group offers a handle for further functionalization, making it a versatile precursor in medicinal chemistry programs.

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