256455-94-4

Basic information

• Product Name: methyl 4,6-O-(phenylmethylene)-3-deoxy-3-(4-morpholinyl)-α-D-altro-pyranoside
• Synonyms: methyl 4,6-O-(phenylmethylene)-3-deoxy-3-(4-morpholinyl)-α-D-altro-pyranoside
• CAS NO: 256455-94-4
• Molecular Weight: 351.4
• Mol File: 256455-94-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 4,6-O-(phenylmethylene)-3-deoxy-3-(4-morpholinyl)-α-D-altro-pyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,6-O-(phenylmethylene)-3-deoxy-3-(4-morpholinyl)-α-D-altro-pyranoside(256455-94-4)
• EPA Substance Registry System: methyl 4,6-O-(phenylmethylene)-3-deoxy-3-(4-morpholinyl)-α-D-altro-pyranoside(256455-94-4)

Safety Data

• Hazardous Substances Data: 256455-94-4(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 3150-15-0 methyl 2,3-anhydro-4,6-O-benzilidene-α-D-mannopyranoside 

Downstream Products

• 138638-80-9 Methyl 2-O-allyl-4,6-O-benzylidene-3-deoxy-α-D-erythro-hex-2-enopyranoside 
• 135700-48-0 methyl 4,6-O-benzylidene-3-deoxy-3-C-propenyl-α-D-arabino-hexopyranoside-2-ulose 
• 256456-02-7 methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-α-D-erythro-hex-2-enopyranoside 
• 74524-02-0 methyl 4,6-O-(phenylmethylene)-3-deoxy-α-D-erythro-hexopyranoside-2-ulose 
• 256455-99-9 methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-benzoyl-3-(4-morpholinyl)-α-D-altro-pyranoside 
• 256455-98-8 methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-benzyl-3-(4-morpholinyl)-α-D-altro-pyranoside 
• 256456-01-6 methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-2-methylallyl-3-(4-morpholinyl)-α-D-altro-pyranoside 
• 256456-00-5 methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-allyl-3-(4-morpholinyl)-α-D-altro-pyranoside 
• 256455-96-6 methyl 4,6-O-(phenylmethylene)-3-deoxy-2-O-methyl-3-(4-morpholinyl)-α-D-altro-pyranoside 

Relevant articles and documents

Synthesis and application of novel carbohydrate-based ammonium and triazolium salts

The synthesis of nine new carbohydrate-based quaternary ammonium salts and two new triazolium salts starting from d-glucose has been accomplished. Our synthesis utilized the regio- and stereoselective ring opening reaction of 2,3-anhydro sugars by nucleop