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Catalog Number:
16557
CAS Number:
40856-59-5
( S -(-)-α-(Boc-Amino)-γ-butyrolactone
Purity:
≥ 99 % (HPLC chirale, HPLC)
Synonym(s):
Boc-L-homosérine lactone
Documents
$19.73 /1G
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Product Information

(S)-(-)-a-(Boc-Amino)-g-butyrolactone is a versatile compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This compound, also known as tert-butyl N-[(3S)-2-oxooxolan-3-yl]carbamate, features a unique structure that enhances its reactivity and selectivity in chemical reactions. Its ability to serve as a chiral building block makes it particularly valuable in the development of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for creating effective and safe medications.

Researchers and industry professionals appreciate this compound for its role in the synthesis of amino acids and peptides, as well as its application in the production of biologically active molecules. Its stability and ease of handling further contribute to its appeal, allowing for efficient integration into various synthetic pathways. Whether in drug development or agricultural formulations, (S)-(-)-a-(Boc-Amino)-g-butyrolactone stands out as a key ingredient that can enhance product efficacy and performance.

Synonyms
Boc-L-homosérine lactone
CAS Number
40856-59-5
Purity
≥ 99 % (HPLC chirale, HPLC)
Molecular Formula
C 9 H 15 NON 4
Molecular Weight
201.22
MDL Number
MFCD04973958
PubChem ID
3297380
Appearance
Solide blanc à blanc cassé
Optical Rotation
[a] 20 D = 9 ± 2 º (C=1 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-homosérine lactone
CAS Number
40856-59-5
Purity
≥ 99 % (HPLC chirale, HPLC)
Molecular Formula
C 9 H 15 NON 4
Molecular Weight
201.22
MDL Number
MFCD04973958
PubChem ID
3297380
Appearance
Solide blanc à blanc cassé
Optical Rotation
[a] 20 D = 9 ± 2 º (C=1 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-(-)-a-(Boc-Amino)-g-butyrolactone is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Peptide Synthesis: It is commonly used in the synthesis of peptides, providing a stable and protective group that enhances the efficiency of coupling reactions.
  • Biotechnology: In biotechnology, it plays a role in the production of bioactive compounds, aiding in the development of novel therapeutics.
  • Material Science: The compound is explored for its potential applications in creating advanced materials, including biodegradable polymers that can be used in drug delivery systems.
  • Research Tools: Researchers utilize it as a reagent in various chemical reactions, benefiting from its ability to improve yields and selectivity in synthetic pathways.

Citations