200133-20-6

Basic information

• Product Name: di-tert-butyl 3,3'-((2-(((benzyloxy)carbonyl)amino)-2-((3-(tert-butoxy)-3-oxopropoxy)methyl)propane-1,3-diyl)bis(oxy))dipropionate
• Synonyms: di-tert-butyl 3,3'-((2-(((benzyloxy)carbonyl)amino)-2-((3-(tert-butoxy)-3-oxopropoxy)methyl)propane-1,3-diyl)bis(oxy))dipropionate
• CAS NO: 200133-20-6
• Molecular Weight: 639.784
• Mol File: 200133-20-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: di-tert-butyl 3,3'-((2-(((benzyloxy)carbonyl)amino)-2-((3-(tert-butoxy)-3-oxopropoxy)methyl)propane-1,3-diyl)bis(oxy))dipropionate(CAS DataBase Reference)
• NIST Chemistry Reference: di-tert-butyl 3,3'-((2-(((benzyloxy)carbonyl)amino)-2-((3-(tert-butoxy)-3-oxopropoxy)methyl)propane-1,3-diyl)bis(oxy))dipropionate(200133-20-6)
• EPA Substance Registry System: di-tert-butyl 3,3'-((2-(((benzyloxy)carbonyl)amino)-2-((3-(tert-butoxy)-3-oxopropoxy)methyl)propane-1,3-diyl)bis(oxy))dipropionate(200133-20-6)

Safety Data

• Hazardous Substances Data: 200133-20-6(Hazardous Substances Data)

Upstream product

• 200133-15-9 N-(Benzyloxycarbonyl)-tris[((methoxycarbonyl)ethoxy)methyl]aminomethane 
• 166047-75-2 tris[(carboxyethoxy)ethyl](amino)methane trimethyl ester 
• 501-53-1 benzyl chloroformate 
• 1663-39-4 tert-Butyl acrylate 
• 175724-30-8 tris{[2-(tert-butoxycarbonyl)ethoxy]methyl}methylamine 
• 200133-16-0 benzyl N-tris[(2-carboxyethyloxy)methyl]methylcarbamate 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 132491-90-8 3-[2-Amino-3-(2-ethoxycarbonyl-ethoxy)-2-(2-ethoxycarbonyl-ethoxymethyl)-propoxy]-propionic acid ethyl ester 
• 220431-66-3 benzyl N-{tris[2-(ethoxycarbonyl)ethoxymethyl]methyl}carbamate 
• 200133-16-0 benzyl N-tris[(2-carboxyethyloxy)methyl]methylcarbamate 
• 175724-30-8 tris{[2-(tert-butoxycarbonyl)ethoxy]methyl}methylamine 

Relevant articles and documents

Assessing changes in the expression levels of cell surface proteins with a turn-on fluorescent molecular probe

Tri-nitrilotriacetic acid (NTA)-based fluorescent probes were developed and used to image His-tagged-labelled outer membrane protein C (His-OmpC) in liveEscherichia coli. One of these probes was designed to light up upon binding, which provided the means

GALNAC DERIVATIVES

Modified oligonucleotides comprising a GalNAc moiety of the present disclosure along with methods of making and use, e.g., against HBV are disclosed.

Affinity enhancement by dendritic side chains in synthetic carbohydrate receptors

Dendritic side chains have been used to modify the binding environment in anthracene-based synthetic carbohydrate receptors. Control of length, charge, and branching enabled the positioning of side-chain carboxylate groups in such a way that they assisted