2-[2-(2-t-Boc-aminoethoxy]ethoxy]ethyl Bromide

• CAT Number: R003354
• CAS Number: 165963-71-3
• Molecular Formula: C11H22BrNO4
• Molecular Weight: 312.204
• Purity: ≥95%
• Synonyms: N-[2-[2-(2-Bromoethoxy)ethoxy]ethyl]carbamic Acid 1,1-Dimethylethyl Ester; 2-[2-[2-(tert-Butoxycarbonylamino)ethoxy]ethoxy]ethyl Bromide
• Target: PROTAC
• Storage: -20°C
• IUPAC Name: tert-butyl N-[2-[2-(2-bromoethoxy)ethoxy]ethyl]carbamate
• InChI: InChI=1S/C11H22BrNO4/c1-11(2,3)17-10(14)13-5-7-16-9-8-15-6-4-12/h4-9H2,1-3H3,(H,13,14)
• InChIKey: WGWDCMKAMHBDPO-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NCCOCCOCCBr

2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethyl Bromide(CAT: R003354) is a chemical compound used in organic synthesis and protection strategies. Its action target involves the modification and protection of amino groups during chemical reactions. The mode of action includes adding the tert-butyloxycarbonyl (Boc) protecting group to the amino group of 2-[2-(2-aminoethoxy)ethoxy]ethyl bromide, shielding it from unwanted reactions during subsequent chemical reactions. Pharmacologically, 2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethyl bromide itself does not have direct medical applications. Instead, it plays a crucial role in organic synthesis, particularly in peptide and small molecule synthesis, where the Boc protecting group is used to protect and control the reactivity of amino groups.