72079-83-5

Basic information

• Product Name: methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside
• Synonyms: methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside
• CAS NO: 72079-83-5
• Molecular Weight: 348.396
• Mol File: 72079-83-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside(72079-83-5)
• EPA Substance Registry System: methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside(72079-83-5)

Safety Data

• Hazardous Substances Data: 72079-83-5(Hazardous Substances Data)

Upstream product

• 3699-66-9 ethyl 2-diethoxyphosphorylpropionate 
• 66537-92-6 methyl 2,3-anhydro-4,6-benzylidene-α-D-allopyranoside 
• 29668-62-0 methyl 2-(diethoxyphosphoryl)propanoate 

Downstream Products

• 72079-88-0 methyl 6,8-O-benzylidene-2,3,4,5-tetradeoxy-4,5-C-isopropylidene-2-C-methtyl-D-manno-oct-2-(E)-enoate 
• 72079-88-0 methyl 6,8-O-benzylidene-2,3,4,5-tetradeoxy-4,5-C-isopropylidene-2-C-methyl-D-gluco-oct-2-(E)-enoate 
• 72120-99-1 methyl 6,8-O-benzylidene-2,3,4,5-tetradeoxy-4,5-C-isopropylidene-2-C-methyl-D-gluco-oct-2-(Z)-enoate 
• 72079-87-9 4,6-O-benzylidene-2,3-dideoxy-2,3-C-isopropylidene-aldehydo-D-mannose 
• 72120-96-8 4,6-O-benzylidene-2,3-dideoxy-2,3-C-isopropylidene-D-glucose 
• 92464-12-5 methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside 
• 72079-85-7 methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside 
• 92464-17-0 (1aR,3aR,6R,7aS,7bS)-1,1-Dimethyl-6-phenyl-hexahydro-3,5,7-trioxa-cyclopropa[a]naphthalen-2-ol 
• 72079-86-8 methyl 4,6-O-(phenylmethylene)-2,3-dideoxy-2,3-C-isopropylidene-α-D-mannopyranoside 
• 33383-55-0 (+) trans-chrysanthemum dicarboxylic acid 
• 72079-84-6 methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-C--α-D-mannopyranoside 

Relevant articles and documents

Use of Radical Ring-Opening for Introduction of Alkyl and Substituted Alkyl Groups with Stereochemical Control: A Synthetic Application of Cyclopropylcarbinyl Radicals

Cyclopropylcarbinols 2a and 2b (see Scheme I), which are accessible by a number of routes, can be converted into the corresponding radicals 3a and 3b, respectively.These radicals undergo peripheral ring-opening of the cyclopropyl substructure to afford su