2405-69-8

Basic information

• Product Name: 2,3,4-tri-O-benzyl-D-arabinitol
• CAS NO: 2405-69-8
• Molecular Weight: 422.521
• Mol File: 2405-69-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,3,4-tri-O-benzyl-D-arabinitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4-tri-O-benzyl-D-arabinitol(2405-69-8)
• EPA Substance Registry System: 2,3,4-tri-O-benzyl-D-arabinitol(2405-69-8)

Safety Data

• Hazardous Substances Data: 2405-69-8(Hazardous Substances Data)

Upstream product

• 488-81-3 Adonitol 
• 100-44-7 benzyl chloride 
• 96871-07-7 1,5-di-O-tritylxylitol 
• 87-99-0 XYLITOL 
• 2159-34-4 1,5-Di-O-trityl-2,3,4-tri-O-benzyladonitol 
• 18039-26-4 2,3,4-tri-O-benzyloxy-L-arabinopyranose 
• 96871-07-7 1,5-Di-O-trityl-L-arabinitol 
• 7643-75-6 L-(-)-arabitol 

Downstream Products

• 158931-70-5 N-Propyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-imino-L-arabinitol 
• 158931-71-6 N-Butyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-imino-L-arabinitol 
• 158931-72-7 N-Pentyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-imino-L-arabinitol 
• 96236-35-0 2,3,4-tri-O-benzyl-D-lyxose diethyl dithioacetal 
• 138481-64-8 Acetic acid (2R,3S,4S)-2,3,4-tris-benzyloxy-5-oxo-pentyl ester 
• 138481-57-9 Acetic acid (2R,3R,4R)-2,3,4-tris-benzyloxy-5-hydroxy-pentyl ester 
• 138481-60-4 Acetic acid (2R,4R)-5-acetoxy-2,3,4-tris-benzyloxy-pentyl ester 
• 2159-31-1 1,5-Di-O-toluene-p-sulfonyl-2,3,4-tri-O-benzyl-D-arabinitol 
• 138481-57-9 (2S,3R,4R)-1-O-Acetyl-2,3,4-tri-O-benzyladonitol 
• 138481-60-4 1,5-Di-O-acetyl-2,3,4-tri-O-benzyladonitol 

Relevant articles and documents

One-pot cascade synthesis of azabicycles via the nitro-Mannich reaction and N -alkylation

A one-pot, metal-free process for the synthesis of azabicycles is developed. The key transformations involved a cascade of double intramolecular cyclizations via the nitro-Mannich reaction and N-alkylation, providing various ring systems of azabicycles in

Nanomolar versus millimolar inhibition by xylobiose-derived azasugars: Significant differences between two structurally distinct xylanases

The synthesis of xylobiose-derived nitrogen-containing inhibitors of xylanase is described starting with accessible precursors through efficient synthetic schemes. Four disaccharides were identified as powerful competitive inhibitors of the retaining fami

HYDROXYLATED PIPERIDINES: SYNTHESIS OF 1,5-ALKYLIMINO-1,5-DIDEOXY DERIVATIVES OF XYLITOL, D- AND L-ARABINITOL, AND RIBITOL

Direct routes are reported for the synthesis of N-propyl, N-butyl and N-pentyl-1,5-dideoxy-1,5-iminoxylitol (7a,b,c), the analogous derivatives (8a,b,c, and 9a,b,c) of 1,5-dideoxy-1,5-imino-D- and -L-arabinitol, and of N-propyl-1,5-dideoxy-1,5-iminoribito