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CAS 176982-57-3

:

(S)-3-BOC-AMINO-BUTYLAMINE

Description:
(S)-3-BOC-amino-butylamine, with the CAS number 176982-57-3, is a chiral amine that features a tert-butyloxycarbonyl (BOC) protecting group on the amino functional group. This compound is characterized by its structural configuration, which includes a butyl chain and an amino group, making it a valuable intermediate in organic synthesis, particularly in the production of pharmaceuticals and biologically active compounds. The BOC group serves to protect the amine during various chemical reactions, allowing for selective transformations. The presence of the chiral center indicates that this compound can exist in two enantiomeric forms, with the (S)-configuration being of particular interest in asymmetric synthesis. Typically, (S)-3-BOC-amino-butylamine is a solid at room temperature and is soluble in polar organic solvents. Its reactivity is influenced by the amino group, which can participate in nucleophilic reactions, while the BOC group can be removed under acidic conditions to yield the free amine. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis.
Formula:C9H21ClN2O2
InChI:InChI=1/C9H20N2O2/c1-7(5-6-10)11-8(12)13-9(2,3)4/h7H,5-6,10H2,1-4H3,(H,11,12)/t7-/m0/s1
SMILES:C[C@@H](CCN)N=C(O)OC(C)(C)C
Synonyms:
  • Carbamic acid, [(1S)-3-amino-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)
  • tert-butyl [(1S)-3-amino-1-methylpropyl]carbamate
  • 3-N-Boc-butane-1,3-diaMine
  • Carbamic acid, N-[(1S)-3-amino-1-methylpropyl]-, 1,1-dimethylethyl ester
  • carbamate
  • 4-amino-2-(aminomethyl)butanoic acid tert-butyl ester hydrochloride
  • 3-N-Boc-butane-1,3-diamine-HCl
  • (S)-3-Boc-aminobutylamine hydrochloride
  • 3-N-Boc-Butane-1,3-diaMine hydrochloride
  • 3(S)-Boc-aMino-butylaMine
  • See more synonyms
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