39022-34-9

Basic information

• Product Name: 3,6-di-O-p-tolylsulfonyl-2,5-anhydro-L-idofuranose dimethylacetal
• Synonyms: 3,6-di-O-p-tolylsulfonyl-2,5-anhydro-L-idofuranose dimethylacetal
• CAS NO: 39022-34-9
• Molecular Weight: 516.59
• Mol File: 39022-34-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,6-di-O-p-tolylsulfonyl-2,5-anhydro-L-idofuranose dimethylacetal(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-di-O-p-tolylsulfonyl-2,5-anhydro-L-idofuranose dimethylacetal(39022-34-9)
• EPA Substance Registry System: 3,6-di-O-p-tolylsulfonyl-2,5-anhydro-L-idofuranose dimethylacetal(39022-34-9)

Safety Data

• Hazardous Substances Data: 39022-34-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 7022-86-8 1,2-O-Isopropyliden-3,5,6-tri-O-p-toluolsulfonyl-α-D-glucofuranose 

Downstream Products

• 73331-65-4 (αS,2R,5S)-N-tert-butyl-2,5-dihydro-5-methyl-α-benzamido>-2-furanacetamide 
• 73331-66-5 N-[(S)-tert-Butylcarbamoyl-((2R,5S)-5-methyl-2,5-dihydro-furan-2-yl)-methyl]-benzamide 
• 73331-65-4 N-[(R)-tert-Butylcarbamoyl-((2R,5S)-5-methyl-2,5-dihydro-furan-2-yl)-methyl]-N-((R)-1-phenyl-ethyl)-benzamide 
• 75511-64-7 Toluene-4-sulfonic acid (2R,3R,5S)-2-dimethoxymethyl-5-methyl-tetrahydro-furan-3-yl ester 
• 73365-46-5 N-[(R)-tert-Butylcarbamoyl-((2R,5S)-5-methyl-2,5-dihydro-furan-2-yl)-methyl]-benzamide 
• 67492-40-4 2,5-Anhydro-4,6-di-Se-phenyl-4,6-diseleno-L-mannose Dimethyl Acetal 
• 39706-33-7 2,5-anhydro-3,4,6-tri-O-benzoyl-L-mannose dimethyl acetal 
• 103739-85-1 2,5-anhydro-2,4,6-tri-O-benzoyl-L-mannose 
• 67492-43-7 2,5:3,4-dianhydro-L-talose dimethyl acetal p-toluenesulfonate 
• 67492-43-7 6-O-p-tolylsulfonyl-2,5:3,4-dianhydro-L-talofuranose dimethylacetal 
• 103739-84-0 2,5-anhydro-4,6-di-O-benzoyl-L-mannose dimethyl acetal 

Relevant articles and documents

Stereoselective synthesis of 4-deoxy-4-nucleobase-2,5-anhydro-L-mannitol derivatives

2,5:3,4-Dianhydro-L-talofuranose dimethylacetal 7 was synthesized from D-glucose in 7 steps. A series of 4-deoxy-4-nucleobase-2,5-anhydro-L-mannitols 13-16 were synthesized regioselectively from 7 in good yields. 6-O-p-Tolylsulfonyl-2,5:3,4-dianhydro-L-ta