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Catalog Number:
14107
CAS Number:
67385-09-5
2-(Boc-amino)etanotiol
Purity:
≥ 98% (GC)
Synonym(s):
N- (2-mercaptoetil)carbamato de terc -butilo, Boc-cisteamina, N - terc -butoxicarbonil-2-aminoetanotiol
Documents
$72.31 /5 ml
Tamaño
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Product Information

2-(Boc-amino)ethanethiol is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This compound features a tert-butyl carbamate protecting group, which makes it particularly valuable for the selective modification of amino groups in various chemical reactions. Its unique structure allows for the introduction of thiol functionalities, making it an essential building block in the development of pharmaceuticals and agrochemicals. Researchers often leverage its reactivity in peptide synthesis and the preparation of complex organic molecules, enhancing the efficiency of their synthetic pathways.

In addition to its applications in synthesis, 2-(Boc-amino)ethanethiol has shown promise in the development of novel therapeutic agents, particularly in the realm of targeted drug delivery systems. Its ability to form stable linkages with other molecular entities allows for the creation of innovative compounds with improved bioavailability and efficacy. This compound stands out due to its ease of handling and compatibility with various reaction conditions, making it a preferred choice for both academic and industrial chemists seeking reliable and effective reagents for their research.

Synonyms
N- (2-mercaptoetil)carbamato de terc -butilo, Boc-cisteamina, N - terc -butoxicarbonil-2-aminoetanotiol
CAS Number
67385-09-5
Purity
≥ 98% (GC)
Molecular Formula
C7H15NO2S
Molecular Weight
177.26
MDL Number
MFCD00274335
PubChem ID
3017761
Density
1,049 g/mL a 20 °C
Appearance
Sólido/líquido de color canela o amarillo, de bajo punto de fusión.
Boiling Point
68 °C/0,3 mmHg
Refractive Index
número 20/D 1.474
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
N- (2-mercaptoetil)carbamato de terc -butilo, Boc-cisteamina, N - terc -butoxicarbonil-2-aminoetanotiol
CAS Number
67385-09-5
Purity
≥ 98% (GC)
Molecular Formula
C7H15NO2S
Molecular Weight
177.26
MDL Number
MFCD00274335
PubChem ID
3017761
Density
1,049 g/mL a 20 °C
Appearance
Sólido/líquido de color canela o amarillo, de bajo punto de fusión.
Boiling Point
68 °C/0,3 mmHg
Refractive Index
número 20/D 1.474
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(Boc-amino)ethanethiol is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting the rest of the peptide chain. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: It plays a role in the design of novel drugs, particularly in creating compounds with improved bioavailability and stability, which are essential for effective therapeutic agents.
  • Bioconjugation: The thiol group in this compound facilitates bioconjugation reactions, enabling researchers to attach biomolecules to surfaces or other molecules, which is vital in diagnostics and targeted drug delivery systems.
  • Research in Neuroscience: It is used in the study of neurotransmitter systems, helping scientists understand the mechanisms of action of various neuroactive compounds, which can lead to breakthroughs in treating neurological disorders.
  • Material Science: This chemical is applied in the development of functionalized surfaces and materials, enhancing properties like adhesion and biocompatibility, which are important in biomedical applications.

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