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CAS 162955-48-8

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(S)-(-)-2-(BOC-amino)-1,5-Pentanediol

Description:
(S)-(-)-2-(BOC-amino)-1,5-Pentanediol is a chiral compound characterized by the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amino functional group, which is crucial for its application in organic synthesis and pharmaceutical chemistry. This compound features a pentanediol backbone, indicating the presence of two hydroxyl (-OH) groups, which contribute to its hydrophilicity and potential for hydrogen bonding. The stereochemistry denoted by (S)-(-) indicates that it is the S-enantiomer, which can exhibit different biological activity compared to its R counterpart. The BOC group serves to protect the amino group during chemical reactions, allowing for selective modifications of other functional groups. This compound is typically used in the synthesis of peptides and other biologically active molecules, making it valuable in medicinal chemistry. Its solubility and reactivity can be influenced by the presence of the hydroxyl groups and the BOC protecting group, making it a versatile intermediate in synthetic pathways.
Formula:C10H21NO4
InChI:InChI=1/C10H21NO4/c1-10(2,3)15-9(14)11-8(7-13)5-4-6-12/h8,12-13H,4-7H2,1-3H3,(H,11,14)/t8-/m0/s1
Synonyms:
  • (S)-tert-butyl 1,5-dihydroxypentan-2-yl carbamate
  • tert-butyl [(1S)-4-hydroxy-1-(hydroxymethyl)butyl]carbamate
  • (S)-(-)-2-(N-Boc-Amino)-1,5-Pentanediol
  • tert-butyl(S)-1,5-dihydroxypentan-2-ylcarbamate
  • Alogliptin Impurity 61
  • (2S)-2-methylpentane-1,5-diol
  • Carbamic acid, N-[(1S)-4-hydroxy-1-(hydroxymethyl)butyl]-, 1,1-dimethylethyl ester
  • Carbamic acid, [(1S)-4-hydroxy-1-(hydroxymethyl)butyl]-, 1,1-dimethylethyl
  • (S)-(-)-2-(BOC-AMINO)-1,5-PENTANEDIOL USP/EP/BP
  • Boc-Nva(OH)-ol
  • (S)-(-)-2-(BOC-AMINO)-1,5-PENTANEDIOL
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