198417-69-5

Basic information

• Product Name: Carbamic acid, [(1R)-2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester
• CAS NO: 198417-69-5
• Molecular Formula: C24H35NO4Si
• Molecular Weight: 429.632
• Mol File: 198417-69-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [(1R)-2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [(1R)-2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester(198417-69-5)
• EPA Substance Registry System: Carbamic acid, [(1R)-2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester(198417-69-5)

Safety Data

• Hazardous Substances Data: 198417-69-5(Hazardous Substances Data)

Upstream product

• 70930-18-6 ethyl (S)-2-[(tert-butoxycarbonyl)amino]-3-hydroxypropanoate 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 24424-99-5 di-tert-butyl dicarbonate 
• 159846-14-7 methyl (2S)-3-(2,2-dimethyl-1,1-diphenyl-1-silapropoxy)-2-[(tert-butoxy)carbonylamino]propanoate 

Downstream Products

• 885321-31-3 (R)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-(tert-butyldiphenylsilyloxy)propoxy)acetate 

Relevant articles and documents

TRICYCLIC COMPOUNDS AND THEIR USE

Tricyclic compounds and their use are provided. More specifically, tricyclic compounds, pharmaceutical compositions containing them, methods for preparing them, and their use in therapy are also provided.

Pseudoenantiomeric glycoclusters: Synthesis and testing of heterobivalency in carbohydrate-protein interactions

Multivalent carbohydrate-protein interactions are key events in cell recognition processes and have been extensively studied by means of synthetic glycomimetics. To date, frequently the valency, i.e. the multiplicity of the ligand attached to a polyvalent

Facile Route to 3,5-Disubstituted Morpholines: Enantioselective Synthesis of O-Protected trans-3,5-Bis(hydroxymethyl)morpholines

(Equation presented) trans-3,5-Bis(benzyl/terf-butyldiphenylsilyloxymethyl) morpholines, promising candidates for the C2-symmetric class of chiral reagents, were prepared with excellent optical purity. A key step in the synthesis is the couplin