Cas no 485800-29-1 (tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate)

Tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate is a protected amine derivative featuring a disulfide linkage, making it a valuable intermediate in organic synthesis and bioconjugation. The tert-butyloxycarbonyl (Boc) group provides selective amine protection, enabling controlled deprotection under mild acidic conditions. The disulfide bridge offers reversible reactivity, facilitating applications in peptide chemistry, crosslinking, and drug delivery systems. This compound’s stability and functional versatility make it suitable for constructing complex molecular architectures, particularly in pharmaceutical and biochemical research. Its well-defined reactivity profile ensures reproducibility in synthetic workflows, while the dual functionality (amine and disulfide) allows for tailored modifications in target-oriented synthesis.
tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate structure
485800-29-1 structure
Product Name:tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate
CAS No:485800-29-1
MF:C10H22N2O2S2
MW:266.42388010025
CID:2678638
PubChem ID:59035444
Update Time:2025-06-12

tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate Chemical and Physical Properties

Names and Identifiers

    • 485800-29-1
    • SCHEMBL5182157
    • 967-702-5
    • tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate
    • tert-butylN-{2-[(3-aminopropyl)disulfanyl]ethyl}carbamate
    • EN300-7545051
    • tert-butyl N-{2-[(3-aminopropyl)disulfanyl]ethyl}carbamate
    • tert-butyl N-[2-(3-aminopropyldisulfanyl)ethyl]carbamate
    • Inchi: 1S/C10H22N2O2S2/c1-10(2,3)14-9(13)12-6-8-16-15-7-4-5-11/h4-8,11H2,1-3H3,(H,12,13)
    • InChI Key: LBLRQRCRRGHDPW-UHFFFAOYSA-N
    • SMILES: S(CCCN)SCCNC(=O)OC(C)(C)C

Computed Properties

  • Exact Mass: 266.11227030Da
  • Monoisotopic Mass: 266.11227030Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 9
  • Complexity: 196
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1
  • Topological Polar Surface Area: 115?2

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Additional information on tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate

Professional Introduction to Compound with CAS No. 485800-29-1 and Product Name: *tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate*

Compound with the CAS number 485800-29-1 and the product name tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate represents a significant advancement in the field of chemical biology and pharmaceutical research. This compound, characterized by its unique structural composition, has garnered considerable attention due to its potential applications in drug development and therapeutic interventions.

The molecular structure of this compound features a tert-butyl group attached to a carbamate moiety, which is further linked to an ethyl chain terminated by a disulfanyl group. This configuration imparts distinct chemical properties that make it particularly valuable for synthetic chemistry and medicinal applications. The presence of the (3-aminopropyl)disulfanyl moiety introduces both reactive sites and steric hindrance, which can be exploited in designing molecules with specific biological activities.

In recent years, there has been growing interest in the development of novel compounds that can modulate biological pathways associated with various diseases. The carbamate functional group, in particular, has been extensively studied for its role in drug design due to its ability to form stable bonds with biological targets. This compound’s structure suggests that it may interact with enzymes or receptors in a manner that could lead to therapeutic effects.

One of the most compelling aspects of this compound is its potential application in the development of targeted therapies. The disulfanyl group, known for its ability to cross-link proteins, could be particularly useful in creating molecules that induce protein aggregation or modulate protein-protein interactions. Such mechanisms have been explored in the treatment of neurodegenerative diseases, where protein misfolding and aggregation play a critical role.

The tert-butyl group, on the other hand, provides steric bulk that can influence the compound’s solubility and bioavailability. This feature is crucial in pharmaceutical design, as it can affect how well a drug is absorbed and distributed within the body. By optimizing the size and placement of this group, researchers can fine-tune the pharmacokinetic properties of the compound.

Recent studies have highlighted the importance of disulfanyl-containing compounds in medicinal chemistry. These compounds have shown promise in various therapeutic areas, including anti-inflammatory and anti-cancer applications. The ability of disulfanyl groups to form stable disulfide bonds has been exploited to create molecules that can selectively target diseased cells while minimizing side effects on healthy tissues.

The synthesis of this compound involves multiple steps, each requiring careful optimization to ensure high yield and purity. Advanced synthetic techniques, such as palladium-catalyzed cross-coupling reactions and organometallic chemistry, have been employed to construct the complex molecular framework. These methods not only enhance the efficiency of synthesis but also allow for greater control over the stereochemistry of the final product.

In conclusion, compound with CAS No. 485800-29-1 and product name *tert-butyl N-(2-((3-aminopropyl)disulfanyl)ethyl)carbamate* represents a promising candidate for further research and development in pharmaceuticals. Its unique structural features offer numerous possibilities for designing molecules with tailored biological activities. As research continues to uncover new applications for this class of compounds, it is likely that we will see more innovative therapies emerge based on their chemical properties.

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