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CAS 150736-72-4

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N-Boc-(S)-2-Amino-1-Butanol

Description:
N-Boc-(S)-2-Amino-1-Butanol is a chiral amino alcohol that features a tert-butyloxycarbonyl (Boc) protecting group on the amine functional group. This compound is characterized by its ability to participate in various chemical reactions due to the presence of both an amino group and a hydroxyl group, making it a valuable intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. The Boc group serves to protect the amine during synthetic procedures, allowing for selective reactions to occur at other functional sites. The (S) configuration indicates that it is one of the enantiomers of 2-amino-1-butanol, which can influence its biological activity and interactions. N-Boc-(S)-2-Amino-1-Butanol is typically a white to off-white solid and is soluble in polar solvents. Its stability and reactivity make it a useful building block in asymmetric synthesis and medicinal chemistry, where chirality plays a crucial role in the efficacy of drug candidates.
Formula:C9H19NO3
InChI:InChI=1/C9H19NO3/c1-5-7(6-11)10-8(12)13-9(2,3)4/h7,11H,5-6H2,1-4H3,(H,10,12)/t7-/m0/s1
SMILES:CC[C@@H](CO)N=C(O)OC(C)(C)C
Synonyms:
  • Carbamic acid, [(1S)-1-(hydroxymethyl)propyl]-, 1,1-dimethylethyl ester
  • tert-butyl [(2S)-1-hydroxybutan-2-yl]carbamate
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