Description

(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate (CAS: 87694-49-3) is a high-purity, chiral organic compound widely utilized in peptide synthesis and pharmaceutical research. With the molecular formula C₁₀H₂₀N₂O₄, this Boc-protected alanine derivative features a methoxy-methyl amide (Weinreb amide) group, making it a valuable intermediate for controlled carbonyl transformations. Ideal for researchers and scientists, this product is rigorously tested for quality, ensuring consistent performance in complex synthetic pathways. Suitable for use in medicinal chemistry, asymmetric synthesis, and as a building block for bioactive molecules. Available in various quantities to meet both laboratory and industrial-scale demands.

Properties

• CAS Number: 87694-49-3
• Complexity: 260
• IUPAC Name: tert-butyl N-[(1S)-2-[methoxy(methyl)amino]-1-methyl-2-oxo-ethyl]carbamate
• InChI: InChI=1S/C10H20N2O4/c1-7(8(13)12(5)15-6)11-9(14)16-10(2,3)4/h7H,1-6H3,(H,11,14)/t7-/m0/s1
• InChI Key: PWQIGBOSLQHOBT-ZETCQYMHSA-N
• Exact Mass: 232.14230712
• Molecular Formula: C10H20N2O4
• Molecular Weight: 232.28
• SMILES: C[C@@H](C(=O)N(C)OC)NC(=O)OC(C)(C)C
• Topological: 67.9
• Monoisotopic Mass: 232.14230712
• Synonyms: 87694-49-3, Boc-Ala-NMe(OMe), BOC-ALA-N(OCH3)CH3, (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate, N-(tert-Butoxycarbonyl)-L-alanine N’-methoxy-N’-methylamide, (2S)-2-[(tert-butoxy)carbonylamino]-N-methoxy-N-methylpropanamide, MFCD00151859, TERT-BUTYL N-[(1S)-1-[METHOXY(METHYL)CARBAMOYL]ETHYL]CARBAMATE, (S)-TERT-BUTYL 1-(METHOXY(METHYL)AMINO)-1-OXOPROPAN-2-YLCARBAMATE, SCHEMBL153320, PWQIGBOSLQHOBT-ZETCQYMHSA-N, BCP15922, CS-M3456, AKOS008864945, TS-7217, s10784, AC-30244, HY-41650, PD196000, B6019, ST51038390, EN300-173575, N2-(tert-butoxycarbonyl)-N-methoxy-N-methylalaninamide, tert-butyl {(15)-1-[methoxy(methyl)carbamoyl]ethyl}carbamate, tert-butyl{(1S)-1-[methoxy(methyl)carbamoyl]ethyl}carbamate, (S)-N-methoxy-N-methyl-2-(tert-butoxycarbonylamino)propionamide, (S)-t-butyl(1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate, (S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-yl-carbamate, (S)-tert-butyl(1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate, N-(tert-Butoxycarbonyl)-L-alanine N’-methoxy-N’-methylamide, 98%, N2-(TERT-BUTOXYCARBONYL)-N-METHOXY-N-METHYL-L-ALANINAMIDE, t-butyl N-{(1S)-2-[methoxy(methyl)amino]-1-methyl-2-oxoethyl}carbamate, tert-butyl (1S)-2-[methoxy(methyl)amino]-1-methyl-2-oxoethylcarbamate, tert-butyl N-[(2S)-1-(methoxy-methylamino)-1-oxopropan-2-yl]carbamate, tert-butyl N-[(2S)-1-[methoxy(methyl)amino]-1-oxopropan-2-yl]carbamate, tert-butyl{(1S)-2-[methoxy(methyl)amino]-1-methyl-2-oxo ethyl}carbamate, tert-butyl N-[(1S)-2-[methoxy(methyl)amino]-1-methyl-2-oxo-ethyl]carbamate

This compound serves as a versatile intermediate in peptide synthesis, particularly for introducing chiral alanine residues under mild conditions. Its Weinreb amide functionality enables selective conversion to aldehydes or ketones, facilitating complex molecular constructions. Researchers leverage its Boc-protected amine for orthogonal deprotection strategies in multi-step syntheses. It is also employed in the development of protease inhibitors and other pharmacologically active compounds.

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