Atomfair N-Boc-3-bromo-L-alanine Methyl Ester C9H16BrNO4 CAS 175844-11-8

Description

N-Boc-3-bromo-L-alanine Methyl Ester (CAS No. 175844-11-8) is a high-purity, chiral organic compound with the molecular formula C₉H₁₆BrNO₄. This Boc-protected derivative of L-alanine features a bromine substituent at the 3-position and a methyl ester group, making it a versatile intermediate in peptide synthesis and medicinal chemistry. The compound is characterized by its excellent stability under standard storage conditions and its compatibility with a wide range of organic reactions. Ideal for researchers and scientists, this product is rigorously tested for purity and consistency, ensuring reliable performance in synthetic applications. Available in various quantities to suit laboratory-scale and industrial needs.

Properties

• CAS Number: 175844-11-8
• Complexity: 237
• IUPAC Name: methyl (2R)-3-bromo-2-(tert-butoxycarbonylamino)propanoate
• InChI: InChI=1S/C9H16BrNO4/c1-9(2,3)15-8(13)11-6(5-10)7(12)14-4/h6H,5H2,1-4H3,(H,11,13)/t6-/m0/s1
• InChI Key: ODLDPRMMKCMNMD-LURJTMIESA-N
• Exact Mass: 281.02627
• Molecular Formula: C9H16BrNO4
• Molecular Weight: 282.13
• SMILES: CC(C)(C)OC(=O)N[C@@H](CBr)C(=O)OC
• Topological: 64.6
• Monoisotopic Mass: 281.02627
• Synonyms: 175844-11-8, N-Boc-3-bromo-L-alanine Methyl Ester, (R)-Methyl 3-bromo-2-((tert-butoxycarbonyl)amino)propanoate, Alanine, 3-bromo-N-[(1,1-dimethylethoxy)carbonyl]-, methyl ester, methyl (2R)-3-bromo-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate, (R)-Boc-3-bromoalanine methyl ester, MFCD12546209, 3-Bromo-N-Boc-L-alanine methyl ester, (R)?-?Methyl 3-?Bromo-?2-?((tert-?butoxycarbonyl)?amino)?propanoate, SCHEMBL24073146, methyl (R)-3-bromo-2-((tert-butoxycarbonyl)amino)propanoate, N-Boc-3-bromo-L-alanineMethylEster, AC2352, AKOS027323787, AC-29764, CS-12406, DB-136472, CS-0068184, EN300-6477068, methyl (2R)-3-bromo-2-{[(tert-butoxy)carbonyl]amino}propanoate

Application

N-Boc-3-bromo-L-alanine Methyl Ester is widely used as a key building block in the synthesis of modified peptides and peptidomimetics. Its reactive bromine moiety allows for further functionalization, enabling the introduction of diverse side chains. This compound is particularly valuable in the development of pharmaceutical agents and bioactive molecules. Researchers also utilize it in the study of enzyme mechanisms and protein engineering.

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.