651736-08-2

Basic information

• Product Name: methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime
• Synonyms: methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime
• CAS NO: 651736-08-2
• Molecular Weight: 295.292
• Mol File: 651736-08-2.mol

Chemical Properties

• CAS DataBase Reference: methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime(651736-08-2)
• EPA Substance Registry System: methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime(651736-08-2)

Safety Data

• Hazardous Substances Data: 651736-08-2(Hazardous Substances Data)

Upstream product

• 128657-58-9 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 

Downstream Products

• 116561-28-5 methyl 2-amino-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside 
• 128657-58-9 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 848477-39-4 methyl 4,6-O-benzylidene-2-deoxy-2-(4-morpholinyl)-α-D-ribo-hexopyranoside-3-ulose 
• 651735-90-9 methyl 4,6-O-benzylidene-2-deoxy-2-(4-morpholinyl)-α-D-glucopyranoside 
• 169873-65-8 methyl 4,6-O-benzylidene-2-deoxy-2-N-ethylamino-α-D-glucopyranoside 
• 651735-98-7 methyl 2-amino-3-O-trimethylsilyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 651736-02-6 methyl 2-N-benzylamino-4,6-O-benzylidene-2-deoxy-α-D-ribohexopyranoside-3-ulose 
• 169873-66-9 methyl 2-N-benzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 651735-95-4 methyl 2-N-benzylamino-3-O-trimethylsilyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 651735-94-3 methyl 2-N-benzylamino-3-O-trimethylsilyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 651736-04-8 methyl 2,2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-ribo-hexopyranoside-3-ulose 
• 651735-96-5 methyl 2-N,N-dibenzylamino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 651735-99-8 methyl 2,2-N-dibenzylamino-3-O-trimethylsilyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 

Relevant articles and documents

Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc-aldehyde additions.

The ready construction of 24 stereochemically and functionally diverse carbohydrate ligand structures from a core D-glucosamine scaffold has allowed the evaluation of broad ranging structure activity relationships in ligand accelerated zincate additions t

Carbohydrate-derived aminoalcohol ligands for asymmetric Reformatsky reactions

Members of a family of functionally and stereochemically diverse d-glucosamine-derived tertiary aminoalcohol ligands have been used to promote the asymmetric Reformatsky reaction. The β-hydroxyester product tert-butyl 3-phenyl-3-hydroxy-propanoate was obt