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Catalog Number:
14459
CAS Number:
959582-93-5
R)-Boc-4-amino-6-methylthio-hexanoic acid
Purity:
≥ 97% (HPLC)
Documents
$161.64 /100MG
Pack Size Availability Price
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Product Information

(R)-Boc-4-amino-6-methylthio-hexanoic acid is a versatile compound widely utilized in the fields of medicinal chemistry and peptide synthesis. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal building block for the synthesis of complex peptides and pharmaceuticals. Its unique structure, characterized by the presence of a methylthio group, provides specific functionalities that can be leveraged in drug development, particularly in the design of inhibitors and modulators for various biological targets.

Researchers and industry professionals appreciate (R)-Boc-4-amino-6-methylthio-hexanoic acid for its ability to facilitate the introduction of sulfur-containing moieties into peptide sequences, which can significantly influence the pharmacokinetic and pharmacodynamic properties of the resulting compounds. This compound is particularly valuable in the synthesis of bioactive peptides, offering enhanced solubility and stability. Its applications extend to the development of therapeutics in oncology and infectious diseases, where tailored peptide sequences can lead to improved efficacy and reduced side effects.

CAS Number
959582-93-5
Purity
≥ 97% (HPLC)
Molecular Formula
C12H23NO4S
Molecular Weight
277.38
MDL Number
MFCD06410964
Appearance
White powder
Optical Rotation
[a]D20 = +3 ± 0.5º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
CAS Number
959582-93-5
Purity
≥ 97% (HPLC)
Molecular Formula
C12H23NO4S
Molecular Weight
277.38
MDL Number
MFCD06410964
Appearance
White powder
Optical Rotation
[a]D20 = +3 ± 0.5º (C=1 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-Boc-4-amino-6-methylthio-hexanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of pharmaceuticals. Its Boc (tert-butyloxycarbonyl) protection group allows for selective deprotection, facilitating the creation of complex peptide structures.
  • Drug Development: It plays a significant role in the design of novel therapeutic agents, especially in the field of anti-cancer and anti-inflammatory drugs, by modifying biological activity and enhancing efficacy.
  • Biotechnology: The compound is used in the production of bioconjugates, which are essential for creating targeted drug delivery systems, improving the precision of treatments in various medical applications.
  • Research in Neuroscience: It is utilized in studies exploring neuroprotective agents, contributing to the understanding of neurological disorders and potential treatments.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential benefits in skin care products, particularly for formulations aimed at improving skin health and appearance.

Citations