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CAS 709665-73-6

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(4-Bromophenyl)-tert-butoxycarbonylaminoacetic acid methyl ester

Description:
(4-Bromophenyl)-tert-butoxycarbonylaminoacetic acid methyl ester is a chemical compound characterized by its complex structure, which includes a bromophenyl group, a tert-butoxycarbonyl (Boc) protecting group, and an aminoacetic acid moiety. The presence of the bromine atom in the para position of the phenyl ring contributes to its reactivity and potential applications in organic synthesis. The tert-butoxycarbonyl group serves as a protective group for the amine, facilitating the selective functionalization of the molecule during synthetic processes. This compound is typically used in peptide synthesis and medicinal chemistry due to its ability to form stable intermediates. Its methyl ester functionality enhances lipophilicity, which can influence its bioavailability and pharmacokinetic properties. Additionally, the compound's structure suggests potential interactions with biological targets, making it of interest in drug development. As with many organic compounds, handling should be done with care, considering safety protocols due to the presence of bromine and other reactive functional groups.
Formula:C14H18BrNO4
InChI:InChI=1/C14H18BrNO4/c1-13(2,3)20-12(18)14(16,11(17)19-4)9-5-7-10(15)8-6-9/h5-8H,16H2,1-4H3
SMILES:CC(C)(C)OC(=O)C(c1ccc(cc1)Br)(C(=O)OC)N
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