1528459-54-2

Basic information

• Product Name: N-(3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)-4-(3-tosyl-2-(tosylmethyl)propanoyl)benzamide
• Synonyms: N-(3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)-4-(3-tosyl-2-(tosylmethyl)propanoyl)benzamide
• CAS NO: 1528459-54-2
• Molecular Weight: 702.89
• Mol File: 1528459-54-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)-4-(3-tosyl-2-(tosylmethyl)propanoyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)-4-(3-tosyl-2-(tosylmethyl)propanoyl)benzamide(1528459-54-2)
• EPA Substance Registry System: N-(3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)-4-(3-tosyl-2-(tosylmethyl)propanoyl)benzamide(1528459-54-2)

Safety Data

• Hazardous Substances Data: 1528459-54-2(Hazardous Substances Data)

Upstream product

• 4246-51-9 4,7,10-trioxa-1,13-diaminotridecane 
• 124243-00-1 4-[2,2-bis[(p-tolylsulfonyl)-methyl]acetyl]benzoic acid 
• 1528459-51-9 tert-butyl (1-oxo-1-{4-[3-tosyl-2-(tosylmethyl)propanoyl]phenyl}-6,9,12-trioxa-2-azapentadecan-15-yl)carbamate 
• 586-89-0 4-acetyl-benzoic acid 
• 124242-84-8 1-(p-carboxyphenyl)-3-(piperidin-1-yl)propan-1-one hydrochloride 
• 124242-93-9 4-(3-(p-tolylthio)-2-((p-tolylthio)methyl)propanoyl)benzoic acid 
• 320635-20-9 tert-butyl (3-(2-(2-(3-aminopropoxy)ethoxy)ethoxy)propyl)carbamate 

Downstream Products

• 1528459-57-5 C₆₂H₇₄N₄O₁₅S₄ 
• 1528459-60-0 C₅₅H₆₆N₄O₁₃S₃ 

Relevant articles and documents

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.