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Catalog Number:
31656
CAS Number:
188109-89-9
Boc-cis-4-methylthio-Pro-OH
Purity:
≥ 99% (HPLC)
Synonym(s):
(2S, 4S-Boc-4-methylthio-pyrrolidine-2-carboxylic acid
Documents
$113.87 /100MG
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Product Information

Boc-cis-4-methylthio-Pro-OH is a valuable compound widely utilized in the field of peptide synthesis and medicinal chemistry. This amino acid derivative features a unique Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide structures. Its specific configuration allows for the introduction of sulfur-containing moieties, which can significantly influence the biological activity of peptides.

In practical applications, Boc-cis-4-methylthio-Pro-OH is particularly beneficial in the development of pharmaceuticals, where it can serve as a building block for bioactive peptides and other therapeutic agents. Its ability to facilitate the formation of disulfide bonds and improve the overall efficacy of peptide-based drugs makes it a preferred choice among chemists. Additionally, its compatibility with various coupling reagents and methodologies streamlines the synthesis process, allowing for greater efficiency and yield in laboratory settings.

Synonyms
(2S, 4S-Boc-4-methylthio-pyrrolidine-2-carboxylic acid
CAS Number
188109-89-9
Purity
≥ 99% (HPLC)
Molecular Formula
C11H19NO4S
Molecular Weight
261.34
MDL Number
MFCD23106230
PubChem ID
69673467
Appearance
Off-white powder
Optical Rotation
[a]20D = -54.5 ± 1° (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
(2S, 4S-Boc-4-methylthio-pyrrolidine-2-carboxylic acid
CAS Number
188109-89-9
Purity
≥ 99% (HPLC)
Molecular Formula
C11H19NO4S
Molecular Weight
261.34
MDL Number
MFCD23106230
PubChem ID
69673467
Appearance
Off-white powder
Optical Rotation
[a]20D = -54.5 ± 1° (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-cis-4-methylthio-Pro-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and enhancing yield and purity in the final product.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in creating compounds with improved bioavailability and reduced side effects.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules with drugs or imaging agents, which is crucial in targeted therapies and diagnostics.
  • Research in Organic Chemistry: It is employed in various organic synthesis reactions, providing chemists with a versatile tool for constructing complex molecular architectures.
  • Cosmetic Formulations: Due to its stability and compatibility with other ingredients, it is also explored in cosmetic chemistry for formulating skin care products that require specific active ingredients.

Citations