N-t-Boc-2-bromoethylamine (Technical grade, ~90percent)

• CAT Number: R001750
• CAS Number: 39684-80-5
• Molecular Formula: C7H14BrNO2
• Molecular Weight: 224.10
• Purity: ≥95%
• Synonyms: N-(2-bromoethyl)carbamic Acid 1,1-Dimethylethyl Ester; (2-Bromoethyl)carbamic Acid tert-Butyl Ester; 2-(N-Boc-amino)ethyl Bromide; 2-(tert-Butyloxycarbonylamino)ethyl Bromide; N-(2-Bromoethyl)carbamic Acid tert-Butyl Ester; N-(tert-Butoxycarbonyl)-2-
• Storage: -20°C
• IUPAC Name: tert-butyl N-(2-bromoethyl)carbamate
• InChI: InChI=1S/C7H14BrNO2/c1-7(2,3)11-6(10)9-5-4-8/h4-5H2,1-3H3,(H,9,10)
• InChIKey: TZRQZPMQUXEZMC-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NCCBr

N-t-Boc-2-bromoethylamine (Cat No.: R001750) is a protected bromoalkylamine featuring a tert-butoxycarbonyl (t-Boc) group on the nitrogen and a reactive bromine atom on the ethyl chain. The t-Boc group stabilizes the amine, preventing unwanted side reactions during synthesis. This compound is widely used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. The bromoethyl moiety enables nucleophilic substitution, allowing it to be incorporated into larger structures such as peptides, heterocycles, or functionalized polymers.