Description

tert-Butyl (3-bromopyridin-4-yl)carbamate (CAS No. 257937-08-9) is a high-purity synthetic intermediate widely utilized in pharmaceutical and agrochemical research. This compound, with the molecular formula C₁₀H₁₃BrN₂O₂, features a pyridine core functionalized with a bromo substituent and a tert-butoxycarbonyl (Boc) protected amine group. Its robust stability and versatile reactivity make it an essential building block for the synthesis of heterocyclic compounds, kinase inhibitors, and bioactive molecules. Packaged under inert conditions to ensure maximum shelf life, this reagent is ideal for demanding laboratory applications. Available in quantities ranging from milligrams to kilograms, it meets the stringent requirements of industrial and academic researchers.

Properties

• CAS Number: 257937-08-9
• Complexity: 228
• IUPAC Name: tert-butyl N-(3-bromo-4-pyridyl)carbamate
• InChI: InChI=1S/C10H13BrN2O2/c1-10(2,3)15-9(14)13-8-4-5-12-6-7(8)11/h4-6H,1-3H3,(H,12,13,14)
• InChI Key: RPPLNTUECLIOOI-UHFFFAOYSA-N
• Exact Mass: 272.01604
• Molecular Formula: C10H13BrN2O2
• Molecular Weight: 273.13
• SMILES: CC(C)(C)OC(=O)NC1=C(C=NC=C1)Br
• Topological: 51.2
• Monoisotopic Mass: 272.01604
• Synonyms: 257937-08-9, tert-Butyl (3-bromopyridin-4-yl)carbamate, DTXSID70443829, DTXCID20394650, (3-Bromopyridin-4-yl)carbamic acid tert-butyl ester, Tert-butyl N-(3-bromopyridin-4-yl)carbamate, 4-Bocamino-3-bromopyridine, MFCD01860257, (3-BROMO-PYRIDIN-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER, tert-butyl N-(3-bromo-4-pyridyl)carbamate, (3-Bromo-pyridin-4-yl)carbamic acid tert-butyl ester, tert-Butyl(3-bromopyridin-4-yl)carbamate, SCHEMBL4827917, 4-(Boc-amino)-3-bromopyridine, RPPLNTUECLIOOI-UHFFFAOYSA-N, AKOS015838222, CS-W006803, tert-butyl 3-bromopyridin-4-ylcarbamate, DS-10213, SY109795, DB-001736, A5164, EN300-197757

tert-Butyl (3-bromopyridin-4-yl)carbamate serves as a key intermediate in the synthesis of pharmaceutical candidates, particularly in the development of kinase inhibitors and receptor modulators. Its bromopyridine moiety enables cross-coupling reactions (e.g., Suzuki, Stille) for constructing complex heterocycles. The Boc-protected amine facilitates selective deprotection for further functionalization. Researchers value this compound for its role in medicinal chemistry and drug discovery pipelines.

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