Description
Methyl 4-bromo-6-((tert-butoxycarbonyl)amino)picolinate (CAS No. 885326-87-4) is a high-purity, synthetic organic compound with the molecular formula C12H15BrN2O4. This specialized chemical is a valuable intermediate in pharmaceutical and agrochemical research, particularly in the synthesis of complex heterocyclic compounds. The presence of both bromo and tert-butoxycarbonyl (Boc) protected amino groups on the picolinate scaffold makes it a versatile building block for medicinal chemistry applications. Our product is rigorously tested for identity and purity (typically >95% by HPLC) to ensure consistent performance in your synthetic workflows. Supplied as a white to off-white crystalline solid, it is packaged under inert atmosphere to maximize shelf life and stability.
Key features:
- IUPAC Name: methyl 4-bromo-6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-2-carboxylate
- Molecular Weight: 331.17 g/mol
- Precisely controlled moisture levels (<1% by KF)
- Stored at 2-8°C for long-term stability
- Available in research quantities from milligrams to kilograms
Properties
- CAS Number: 885326-87-4
- Complexity: 343
- IUPAC Name: methyl 4-bromo-6-(tert-butoxycarbonylamino)pyridine-2-carboxylate
- InChI: InChI=1S/C12H15BrN2O4/c1-12(2,3)19-11(17)15-9-6-7(13)5-8(14-9)10(16)18-4/h5-6H,1-4H3,(H,14,15,17)
- InChI Key: AKTYIVKMAJBROD-UHFFFAOYSA-N
- Exact Mass: 330.02152
- Molecular Formula: C12H15BrN2O4
- Molecular Weight: 331.16
- SMILES: CC(C)(C)OC(=O)NC1=CC(=CC(=N1)C(=O)OC)Br
- Topological: 77.5
- Monoisotopic Mass: 330.02152
- Synonyms: 885326-87-4, Methyl 4-bromo-6-((tert-butoxycarbonyl)amino)picolinate, 4-Bromo-6-[(tert-butoxycarbonyl)amino]pyridine-2-carboxylic acid methyl ester, Methyl 4-bromo-6-((tert-butoxycarbonyl)-amino)picolinate, methyl 4-bromo-6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-2-carboxylate, SCHEMBL397093, Methyl4-bromo-6-((tert-butoxycarbonyl)amino)picolinate, DTXSID30648595, AKTYIVKMAJBROD-UHFFFAOYSA-N, AKOS015901532, DB-077874, methyl 4-bromo-6-t-butoxycarbonylamino-pyridine-2-carboxylate, methyl 4-bromo-6-tert-butoxycarbonylaminopyridine-2-carboxylate, METHYL 4-BROMO-6-[(TERT-BUTOXYCARBONYL)AMINO]PYRIDINE-2-CARBOXYLATE
Application
This compound serves as a key intermediate in the synthesis of pharmaceutical candidates, particularly those targeting kinase inhibition. The bromo substituent allows for further functionalization via cross-coupling reactions, while the Boc-protected amino group provides a handle for subsequent deprotection and derivatization. Researchers utilize this building block in the development of novel pyridine-based drug scaffolds. Its structural features make it particularly valuable for constructing molecular libraries in drug discovery programs.
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