525578-70-5

Basic information

• Product Name: Carbamic acid, methyl(2-phenoxyethyl)-, 1,1-dimethylethyl ester
• CAS NO: 525578-70-5
• Molecular Formula: C14H21NO3
• Molecular Weight: 251.326
• Mol File: 525578-70-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, methyl(2-phenoxyethyl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, methyl(2-phenoxyethyl)-, 1,1-dimethylethyl ester(525578-70-5)
• EPA Substance Registry System: Carbamic acid, methyl(2-phenoxyethyl)-, 1,1-dimethylethyl ester(525578-70-5)

Safety Data

• Hazardous Substances Data: 525578-70-5(Hazardous Substances Data)

Upstream product

• 26690-80-2 2-(N-tert-butoxycarbonylamino)ethanol 
• 96628-67-0 2-(tert-butoxycarbonylamino)ethyl methanesulfonate 
• 1758-46-9 2-phenoxyethanamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 921596-28-3 tert-butyl (2-phenoxyethyl)carbamate 
• 74-88-4 methyl iodide 
• 57561-39-4 methyl(2-hydroxyethyl)carbamic acid tert-butyl ester 

Downstream Products

• 85262-76-6 N-methyl-2-phenoxyethanamine hydrochloride 
• 921596-33-0 tert-butyl N-[2-[4-[4'-(hexafluorocyclopent-1-enyl)-3',5'-dimethyl[2,2']bithyophen-5-yl]phenoxy]ethyl]-N-methyl carbamate 
• 921596-31-8 tert-butyl N-methyl-N-[2-[4-(5-iodothiophen-2-yl)phenoxy]ethyl]carbamate 
• 921596-30-7 tert-butyl N-methyl-N-[2-[4-(thiophen-2-yl)phenoxy]ethyl]carbamate 
• 921596-29-4 tert-butyl N-methyl-N-[2-(4-iodophenoxy)ethyl]carbamate 

Relevant articles and documents

PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS.

Copper(II)-catalyzed ether synthesis from aliphatic alcohols and potassium organotrifluoroborate salts

(Matrix presented) A protocol for the copper(II)-catalyzed etherification of aliphatic alcohols under mild and essentially neutral conditions is described. Air- and moisture-stable potassium alkenyl- and aryltrifluoroborate salts undergo cross-coupling with a variety of aliphatic primary and secondary alcohols and phenols, and are tolerant of a range of functional groups. The optimized conditions utilize catalytic copper(II) acetate with 4-(dimethylamino)pyridine as ligand in the presence of 4 A molecular sieves under an atmosphere of oxygen.