320635-20-9

Usage

Uses

Used in Chemical Stabilization:
Tert-butyl (3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)carbamate is used as a stabilizer in chemical processes to prevent unwanted reactions or degradation, capitalizing on the protective nature of the tert-butyl group and the compound's overall molecular structure.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, tert-butyl (3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)carbamate serves as a building block for the synthesis of complex drug molecules, taking advantage of its multifunctional groups to create novel therapeutic agents.
Used in Material Science:
Tert-butyl (3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)carbamate is utilized in material science as a component in the development of new materials with tailored properties, such as improved solubility, stability, or reactivity, due to its unique molecular architecture.
Used in Industrial Inhibitors:
tert-butyl (3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)carbamate is employed as an inhibitor in various industrial applications to control or slow down specific chemical reactions, ensuring process efficiency and product quality by leveraging its stabilizing properties.
Each application takes advantage of the compound's unique structural features and the functionalities provided by its constituent groups, making tert-butyl (3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)carbamate a versatile and valuable asset across different fields.

Upstream product

• 4246-51-9 4,7,10-trioxa-1,13-diaminotridecane 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 1528459-51-9 tert-butyl (1-oxo-1-{4-[3-tosyl-2-(tosylmethyl)propanoyl]phenyl}-6,9,12-trioxa-2-azapentadecan-15-yl)carbamate 
• 1528459-43-9 N-(3-(2-(2-(3-azidopropoxy)ethoxy)ethoxy)propyl)-4-(3-(p-tolylthio)-2-((p-tolylthio) methyl)propanoyl)benzamide 
• 1528459-46-2 N-(3-(2-(2-(3-azidopropoxy)ethoxy)ethoxy)propyl)-4-(3-tosyl-2-(tosylmethyl)propanoyl)benzamide 
• 1162336-72-2 3-(2-(2-(3-azidopropoxy)ethoxy)ethoxy)propan-1-amine 
• 1528459-54-2 N-(3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)-4-(3-tosyl-2-(tosylmethyl)propanoyl)benzamide 
• 1528459-57-5 C₆₂H₇₄N₄O₁₅S₄ 

Relevant academic research and scientific papers

A disulfide intercalator toolbox for the site-directed modification of polypeptides

A disulfide intercalator toolbox was developed for site-specific attachment of a broad variety of functional groups to proteins or peptides under mild, physiological conditions. The peptide hormone somatostatin (SST) served as model compound for intercalation into the available disulfide functionalization schemes starting from the intercalator or the reactive SST precursor before or after bioconjugation. A tetrazole-SST derivative was obtained that undergoes photoinduced cycloaddition in mammalian cells, which was monitored by live-cell imaging.

Flow-mediated synthesis of Boc, Fmoc, and Dd iv monoprotected diamines

A series of monoprotected aliphatic diamines (21 examples) were synthesized via continuous flow methods. The carbamates and enamines were obtained in 45-91% yields using a 0.5 mm diameter PTFE tubular flow reactor. Using readily accessible protecting group precursors, the procedure serves as an attractive alternative to existing batch-mode synthetic routes by providing direct, multigram access to N-Boc-, N-Fmoc-, and N-Ddiv-protected compounds with productivity indexes of 1.2-3.6 g/h.

Novel hydrazone-based and oxime-based fluorescent and chromophoric/pro-fluorescent and pro-chromophoric reagents and linkers

Conjugationally extended hydrazine compositions of the formula (RR2)N(H)n(NH2)n, fluorescent hydrazone compositions of the formula (RR2)NN═C(R1R2), methods of the formation of hydrazones from the reaction of conjugationally extended hydrazines with conjugationally extended carbonyls and methods of their use in assays systems are described. Use of these conjugationally extended hydrazine and oxime compositions for direct calorimetric and fluorometric assays wherein a chromophore or the fluorophore is incorporated into the linker that is positioned between a reactive linking moiety and a biotin molecule. More specifically the linker comprises one molecule of a high affinity binding pair such as for example biotin of the biotin/avidin high affinity binding pair, connected to a spacer molecule such as for example a length of polyethyleneglycol followed by a pro-chromophoric, chromophoric, pro-fluorescent or fluorescent moiety connected to an amino-, thiol- or carbohydrate-reactive moiety such as for example succinimidyl, maleimido or aminoxy group respectively, that may covalently link to a biomolecule.