Description

tert-Butyl ethyl(2-hydroxyethyl)carbamate (CAS No. 152192-95-5) is a high-purity carbamate derivative with the molecular formula C₉H₁₉NO₃. This compound, also known by its IUPAC name tert-butyl N-ethyl-N-(2-hydroxyethyl)carbamate, is a versatile building block in organic synthesis and pharmaceutical research. It features a tert-butyl carbamate (Boc) protecting group, an ethyl substituent, and a 2-hydroxyethyl moiety, making it valuable for controlled functionalization and peptide coupling strategies. The product is supplied as a clear to pale-yellow liquid or low-melting solid, with ≥95% purity (HPLC). Ideal for researchers requiring precise intermediates, it is stored under inert conditions to ensure stability. Suitable for use in medicinal chemistry, proteomics, and advanced material science applications.

Properties

• CAS Number: 152192-95-5
• Complexity: 163
• IUPAC Name: tert-butyl N-ethyl-N-(2-hydroxyethyl)carbamate
• InChI: InChI=1S/C9H19NO3/c1-5-10(6-7-11)8(12)13-9(2,3)4/h11H,5-7H2,1-4H3
• InChI Key: OPSQZIGTEBZROY-UHFFFAOYSA-N
• Exact Mass: 189.13649347
• Molecular Formula: C9H19NO3
• Molecular Weight: 189.25
• SMILES: CCN(CCO)C(=O)OC(C)(C)C
• Topological: 49.8
• Monoisotopic Mass: 189.13649347
• Synonyms: 152192-95-5, tert-Butyl ethyl(2-hydroxyethyl)carbamate, BOC,ET-GLYCINOL, N-Boc-N-ethyl-ethanolamine, tert-butyl N-ethyl-N-(2-hydroxyethyl)carbamate, BOC,ET-N-ET-OH, ETHYL-(2-HYDROXY-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER, MFCD04973117, Carbamic acid,N-ethyl-N-(2-hydroxyethyl)-, 1,1-dimethylethyl ester, 2-[Boc(ethyl)amino]ethanol, SCHEMBL896291, SCHEMBL4164699, DTXSID90565517, OPSQZIGTEBZROY-UHFFFAOYSA-N, AB1207, AKOS010181134, DS-7402, SB33822, SY046762, tert-Butyl (2-hydroxyethyl)ethylcarbamate, CS-0128600, EN300-61945, N-T-BUTYLOXYCARBONYL-N-ETHYL-AMINOETHANOL, TERT-BUTYL ETHYL-(2-HYDROXYETHYL)CARBAMATE, ethyl-(2-hydroxy-ethyl)-carbamic acid t-butyl ester, Ethyl-(2-hydroxyethyl)carbamic acid tert-butyl ester

Application

tert-Butyl ethyl(2-hydroxyethyl)carbamate is widely used as a protected intermediate in peptide synthesis and medicinal chemistry. Its Boc group enables selective deprotection under mild acidic conditions, facilitating stepwise reactions. The compound is also employed in the development of enzyme inhibitors and prodrugs due to its hydroxyl functionality. Researchers utilize it for modifying biomolecules or creating novel polymer precursors. Its stability and reactivity make it a preferred choice for exploratory organic transformations.

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