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CAS 163210-89-7

:

1,1-Dimethylethyl (2S)-4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]butanoate

Description:
1,1-Dimethylethyl (2S)-4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]butanoate, with CAS number 163210-89-7, is a chemical compound characterized by its complex structure, which includes a bromo substituent and a dimethylethyl group. This compound features a butanoate backbone, indicating it is an ester derived from butanoic acid. The presence of the bromo group suggests potential reactivity, making it useful in various synthetic applications. The dimethylethoxycarbonyl group indicates that it may serve as a protecting group in organic synthesis, particularly in peptide chemistry. The stereochemistry at the 2-position is specified as (2S), which is crucial for its biological activity and interaction with enzymes or receptors. Overall, this compound is likely to be of interest in medicinal chemistry and synthetic organic chemistry due to its functional groups and potential applications in drug development or as an intermediate in chemical synthesis.
Formula:C13H24BrNO4
InChI:InChI=1S/C13H24BrNO4/c1-12(2,3)18-10(16)9(7-8-14)15-11(17)19-13(4,5)6/h9H,7-8H2,1-6H3,(H,15,17)/t9-/m0/s1
InChI key:InChIKey=KAHXNHVFTFWYDP-VIFPVBQESA-N
SMILES:[C@H](C(OC(C)(C)C)=O)(NC(OC(C)(C)C)=O)CCBr
Synonyms:
  • 1,1-Dimethylethyl (2S)-4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]butanoate
  • Butanoic acid, 4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2S)-
  • Butanoic acid, 4-bromo-2-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (S)-
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