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Catalog Number:
05465
CAS Number:
41117-66-2
Boc-S-3,4-dimethylbenzyl-L-cysteine
Purity:
≥ 98% (TLC)
Synonym(s):
Boc-L-Cys(3,4-dimethylBzl)-OH
Documents
$58.39 /100MG
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Product Information

Boc-S-3,4-dimethylbenzyl-L-cysteine is a valuable compound widely utilized in the field of medicinal chemistry and peptide synthesis. This compound features a unique structure that incorporates a Boc (tert-butyloxycarbonyl) protecting group, enhancing its stability and reactivity during various chemical reactions. Its distinctive properties make it particularly useful for researchers focused on developing novel therapeutic agents, especially in the synthesis of peptide-based drugs. The presence of the 3,4-dimethylbenzyl group contributes to its lipophilicity, which can improve the bioavailability of the resulting peptides.

In practical applications, Boc-S-3,4-dimethylbenzyl-L-cysteine serves as a key building block in the synthesis of biologically active compounds, including those targeting specific receptors or pathways in disease processes. Its ability to facilitate the formation of disulfide bonds is particularly advantageous in the design of cyclic peptides, which often exhibit enhanced stability and activity. Researchers and industry professionals can leverage this compound to streamline their synthesis processes and enhance the efficacy of their drug candidates.

Synonyms
Boc-L-Cys(3,4-dimethylBzl)-OH
CAS Number
41117-66-2
Purity
≥ 98% (TLC)
Molecular Formula
C17H25NO4S
Molecular Weight
339.46
MDL Number
MFCD00060743
PubChem ID
21393255
Melting Point
72-79 °C
Appearance
White powder
Optical Rotation
[a]D24 = -33 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Cys(3,4-dimethylBzl)-OH
CAS Number
41117-66-2
Purity
≥ 98% (TLC)
Molecular Formula
C17H25NO4S
Molecular Weight
339.46
MDL Number
MFCD00060743
PubChem ID
21393255
Melting Point
72-79 °C
Appearance
White powder
Optical Rotation
[a]D24 = -33 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-S-3,4-dimethylbenzyl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting other functional groups, which is crucial for creating complex peptides.
  • Drug Development: It plays a significant role in the development of pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing the efficacy and safety of new drugs.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted therapies and diagnostic tools.
  • Research in Cancer Therapy: Its unique structure allows for the exploration of new cancer treatment options, as it can be modified to improve the delivery of therapeutic agents directly to tumor cells.
  • Antioxidant Studies: Researchers utilize this compound to study its antioxidant properties, which can lead to the development of new supplements or treatments aimed at reducing oxidative stress in various diseases.

Citations