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CAS 128427-10-1

:

(S)-(-)-2-(Boc-Amino)-1,4-butanediol

Description:
(S)-(-)-2-(Boc-Amino)-1,4-butanediol is a chiral compound characterized by its specific stereochemistry and functional groups. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group for amines, which indicates that this compound is likely used in peptide synthesis or other organic reactions where amine protection is necessary. The presence of the butanediol moiety suggests that it has two hydroxyl (-OH) groups, contributing to its potential solubility in polar solvents and its ability to participate in hydrogen bonding. The compound's chirality, denoted by the (S) configuration, implies that it may exhibit distinct biological activity or reactivity compared to its enantiomer. This compound is often utilized in pharmaceutical chemistry and research due to its structural features, which can influence the pharmacokinetics and pharmacodynamics of drug candidates. Its CAS number, 128427-10-1, allows for precise identification in chemical databases and literature. Overall, (S)-(-)-2-(Boc-Amino)-1,4-butanediol is a valuable intermediate in organic synthesis with specific applications in medicinal chemistry.
Formula:C9H19NO4
InChI:InChI=1/C9H19NO4/c1-9(2,3)14-8(13)10-7(6-12)4-5-11/h7,11-12H,4-6H2,1-3H3,(H,10,13)/t7-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](CCO)CO)O
Synonyms:
  • (S)-(-)-N-Boc-2-Amino-1,4-Butanediol
  • Carbamic Acid, [(1S)-3-Hydroxy-1-(Hydroxymethyl)Propyl]-, 1,1-Dimethylethyl
  • (S)-(-)-2-(Boc-Amino)-1,4-Butendiol
  • (S)-Tert-Butyl 1,4-Dihydroxybutan-2-Ylcarbamate
  • (S)-N-Boc-2-Amino-Butane-1,4-Diol
  • (S)-(3-Hydroxy-1-hydroxymethylpropyl)carbamic acid tert-butyl ester
  • tert-butyl [(1S)-3-hydroxy-1-(hydroxymethyl)propyl]carbamate
  • (S)-tert-butyl (1,4-dihydroxybutan-2-yl) carbamate
  • (S)-(-)-2-(Boc-Amino)-1,4-butanediol
  • (S)-2-N-Boc-aMinobutane-1,4-diol
  • See more synonyms
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