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2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL

Base Information Edit
  • Chemical Name:2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL
  • CAS No.:20204-84-6
  • Molecular Formula:C6H11NO6
  • Molecular Weight:193.156
  • Hs Code.:2932999099
  • Mol file:20204-84-6.mol
2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL

Synonyms:BETA-D-XYLOPYRANOSYL NITROMETHANE;2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL;SS-D-XYLOPYRANOSYL NITROMETHANE,2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL

Suppliers and Price of 2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL 95.00%
  • 5MG
  • $ 500.37
Total 1 raw suppliers
Chemical Property of 2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL Edit
Chemical Property:
  • PSA:115.74000 
  • LogP:-1.73220 
Purity/Quality:

99%min *data from raw suppliers

2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL

There total 3 articles about 2,6-ANHYDRO-1-DEOXY-1-NITRO-3,4,5-TRI-O-ACETYL-D-GULITOL which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Yield given. Multistep reaction;
DOI:10.1016/0008-6215(87)80143-X
Guidance literature:
DOI:10.1021/jo01065a069
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