Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
05296
CAS Number:
56976-06-8
Boc-S- tert -butyl-L-cystéine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Cys(tBu)-OH, Acide boc-( R -2-amino-3-( S - tert -butylthio)butanoïque
Documents
$18.53 /5G
Taille
Request Bulk Quote
Product Information

Boc-S-tert-butyl-L-cysteine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyl protecting group, which enhances its stability and solubility, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds. Its unique structure allows for selective reactions, facilitating the incorporation of sulfur-containing amino acids into peptides, which is crucial for the development of therapeutics targeting various diseases.

In addition to its role in peptide synthesis, Boc-S-tert-butyl-L-cysteine is also valuable in the field of drug discovery, particularly in the design of inhibitors and modulators for various biological pathways. Its ability to serve as a building block for more complex molecules opens up possibilities for innovative drug formulations. Researchers appreciate its ease of use and the efficiency it brings to synthetic processes, making it a preferred choice in both academic and industrial laboratories.

Synonyms
Boc-L-Cys(tBu)-OH, Acide boc-( R -2-amino-3-( S - tert -butylthio)butanoïque
CAS Number
56976-06-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 23 NON 4 S
Molecular Weight
277.4
MDL Number
MFCD00076918
PubChem ID
13817339
Melting Point
86-92 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -16 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-L-Cys(tBu)-OH, Acide boc-( R -2-amino-3-( S - tert -butylthio)butanoïque
CAS Number
56976-06-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 23 NON 4 S
Molecular Weight
277.4
MDL Number
MFCD00076918
PubChem ID
13817339
Melting Point
86-92 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -16 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-S-tert-butyl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for cysteine residues in peptide synthesis, allowing for selective reactions without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing drug efficacy.
  • Bioconjugation: Its unique structure allows for effective bioconjugation techniques, facilitating the attachment of drugs or imaging agents to proteins, which is vital in targeted therapy.
  • Research in Antioxidants: The compound is used in studies related to antioxidants, helping researchers understand the mechanisms of oxidative stress and potential therapeutic interventions.
  • Protein Engineering: It aids in the engineering of proteins with enhanced stability and functionality, which is essential in various biotechnological applications.

Citations