4-Aminobutylcarbamic Acid tert-Butyl Ester

• CAT Number: R045133
• CAS Number: 68076-36-8
• Molecular Formula: C9H20N2O2
• Molecular Weight: 188.27
• Purity: ≥95%
• Synonyms: N-(4-Aminobutyl)carbamic Acid 1,1-Dimethylethyl Ester?(4-Aminobutyl)carbamic Acid 1,1-Dimethylethyl Ester; 1,1-Dimethylethyl (4-aminobutyl)carbamate; 1-Amino-4-[(tert-butoxycarbonyl)amino]butane; 1-[(tert-Butoxycarbonyl)amino]-4-aminobutane; 4-(tert-
• Target: PROTAC Linkers
• Storage: Store at -20°C
• IUPAC Name: tert-butyl N-(4-aminobutyl)carbamate
• InChI: InChI=1S/C9H20N2O2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7,10H2,1-3H3,(H,11,12)
• InChIKey: ZFQWJXFJJZUVPI-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NCCCCN

4-Aminobutylcarbamic acid tert-butyl ester（Cat No.:R045133）is a protected derivative of 4-aminobutylcarbamic acid, featuring a tert-butyl ester group that safeguards the carboxylic acid functionality during synthetic processes. This compound is commonly used as an intermediate in organic and peptide synthesis, particularly in the preparation of polyamines and bioactive molecules. Its tert-butyl protecting group is stable under basic conditions but can be easily removed under acidic environments, facilitating selective deprotection strategies. This versatility makes it a valuable tool in medicinal chemistry and the development of drug-like molecules or linkers for conjugation.