N-tert-Butoxycarbonyl-3-bromopropylamine

• CAT Number: R019330
• CAS Number: 83948-53-2
• Molecular Formula: C8H16BrNO2
• Molecular Weight: 238.12
• Purity: ≥95%
• Synonyms: N-(3-Bromopropyl)carbamic Acid 1,1-Dimethylethyl Ester; (3-Bromopropyl)carbamic acid 1,1-Dimethylethyl Ester; 1,1-Dimethylethyl (3-bromopropyl)carbamate; 1-[(tert-Butoxycarbonyl)amino]-3-bromopropane; 3-(BOC-amino)propyl Bromide; 3-Bromo-N-(tert-buto
• Storage: 2-8°C
• IUPAC Name: tert-butyl N-(3-bromopropyl)carbamate
• InChI: InChI=1S/C8H16BrNO2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6H2,1-3H3,(H,10,11)
• InChIKey: IOKGWQZQCNXXLD-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NCCCBr

N-tert-Butoxycarbonyl-3-bromopropylamine（Cat No.:R019330）, is a chemical compound used in organic synthesis and as a reagent in peptide and pharmaceutical research. It is often referred to as Boc-3-bromopropylamine. This compound consists of a 3-bromopropylamine molecule with a tert-butoxycarbonyl (Boc) protective group attached to the amino group. The Boc group temporarily protects the amine, allowing selective reactions with other functional groups during peptide synthesis. Boc-3-bromopropylamine plays a crucial role in the preparation of complex peptides and pharmaceutical intermediates by facilitating controlled and precise modifications of amino acids, enabling the development of novel drug compounds and bioactive molecules.