261364-71-0

Basic information

• Product Name: {2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethyl}-carbamic acid 2-[3-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-propyl]-3,5-dimethyl-phenyl ester
• Synonyms: {2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethyl}-carbamic acid 2-[3-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-propyl]-3,5-dimethyl-phenyl ester
• CAS NO: 261364-71-0
• Molecular Weight: 596.88
• Mol File: 261364-71-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: {2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethyl}-carbamic acid 2-[3-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-propyl]-3,5-dimethyl-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: {2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethyl}-carbamic acid 2-[3-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-propyl]-3,5-dimethyl-phenyl ester(261364-71-0)
• EPA Substance Registry System: {2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethyl}-carbamic acid 2-[3-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-propyl]-3,5-dimethyl-phenyl ester(261364-71-0)

Safety Data

• Hazardous Substances Data: 261364-71-0(Hazardous Substances Data)

Upstream product

• 134098-64-9 2‐{3‐[(O‐tert‐butyldimethylsilyl)hydroxy]‐1,1‐dimethylpropyl}‐3,5‐dimethylphenol 
• 153086-78-3 tert-butyl {2-[2-(2-aminoethoxy)ethoxy]ethyl}carbamate 

Downstream Products

• 261364-74-3 3-(2-{2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethylcarbamoyloxy}-4,6-dimethyl-phenyl)-3-methyl-butyric acid 
• 261364-73-2 {2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethyl}-carbamic acid 2-(1,1-dimethyl-3-oxo-propyl)-3,5-dimethyl-phenyl ester 
• 261364-72-1 {2-[2-(2-tert-butoxycarbonylamino-ethoxy)-ethoxy]-ethyl}-carbamic acid 2-(3-hydroxy-1,1-dimethyl-propyl)-3,5-dimethyl-phenyl ester 

Relevant articles and documents

Drug delivery systems based on trimethyl lock lactonization: Poly(ethylene glycol) prodrugs of amino-containing compounds

A novel methodology for the synthesis of poly(ethylene glycol) (PEG) prodrugs of amino-containing compounds has been developed which is based on the trimethyl lock lactonization reaction. These PEG-modified double prodrugs are water soluble, and by select