151734-50-8

Basic information

• Product Name: 2-(benzyloxycarbonylamino)-3-hydroxy-2-(hydroxymethyl)propyl acetate
• Synonyms: 2-(benzyloxycarbonylamino)-3-hydroxy-2-(hydroxymethyl)propyl acetate
• CAS NO: 151734-50-8
• Molecular Weight: 297.308
• Mol File: 151734-50-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(benzyloxycarbonylamino)-3-hydroxy-2-(hydroxymethyl)propyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(benzyloxycarbonylamino)-3-hydroxy-2-(hydroxymethyl)propyl acetate(151734-50-8)
• EPA Substance Registry System: 2-(benzyloxycarbonylamino)-3-hydroxy-2-(hydroxymethyl)propyl acetate(151734-50-8)

Safety Data

• Hazardous Substances Data: 151734-50-8(Hazardous Substances Data)

Upstream product

• 1125824-06-7 C₂₁H₂₃NO₆ 
• 420107-80-8 (5-benzyloxycarbonylamino-2,2-dimethyl[1,3]dioxan-5-yl)methanol 
• 102522-48-5 benzyl 1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl carbamate 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 151753-73-0 Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-[2-acetoxymethyl-2-benzyloxycarbonylamino-3-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-propoxy]-tetrahydro-pyran-4-yl ester 

Relevant articles and documents

Truly catalytic and chemoselective cleavage of benzylidene acetal with phosphomolybdic acid supported on silica gel

Phosphomolybdic acid supported on silica gel provides a truly catalytic method for the chemoselective cleavage of benzylidene acetals having sensitive functional groups under mild conditions. It is easy to perform on large scale owing to minimal catalyst loading (0.5 mol-%). Several sensitive functional groups such as TBDPS ether, -OMs, -OAc, allyl ether, N-Boc, N-Fmoc and N-Cbz are stable under the reaction conditions. In addition, benzylidene acetal is selectively cleaved in the presence of isopropylidene ketal. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.