(2-(((1-Chloroethoxy)carbonyl)(methyl)amino)pyridin-3-yl)methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate

• CAT Number: R072888
• CAS Number: 338990-31-1
• PubChem Substance ID: 11281469
• Molecular Formula: C18H26ClN3O6
• Molecular Weight: 415.87
• Purity: ≥95%
• IUPAC Name: [2-[1-chloroethoxycarbonyl(methyl)amino]pyridin-3-yl]methyl 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]acetate
• InChI: InChI=1S/C18H26ClN3O6/c1-12(19)27-17(25)22(6)15-13(8-7-9-20-15)11-26-14(23)10-21(5)16(24)28-18(2,3)4/h7-9,12H,10-11H2,1-6H3
• InChIKey: KXWGVTDANRDXRN-UHFFFAOYSA-N
• SMILES: CC(OC(=O)N(C)C1=C(C=CC=N1)COC(=O)CN(C)C(=O)OC(C)(C)C)Cl

(2-(((1-Chloroethoxy)carbonyl)(methyl)amino)pyridin-3-yl)methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate（Cat No.:R072888）is a synthetically engineered molecule featuring protective carbamate groups such as 1-chloroethoxycarbonyl and tert-butoxycarbonyl (Boc), often used in peptide and medicinal chemistry. Structurally, it combines a pyridine core with esterified and N-methylated amino functionalities, offering sites for selective reaction and molecular modification. It serves as an intermediate in the synthesis of complex bioactive compounds, aiding in controlled functional group transformations. Its reactive sites require moisture-free, inert conditions for stability. Proper storage and handling with protective equipment are essential due to potential reactivity and the presence of halogenated and carbamate moieties.