Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

UDP-N-acetyl-alpha-D-mannosamine

Base Information
  • Chemical Name:UDP-N-acetyl-alpha-D-mannosamine
  • CAS No.:26575-17-7
  • Molecular Formula:C17H27N3O17P2
  • Molecular Weight:607.359
  • Hs Code.:
  • DSSTox Substance ID:DTXSID701313724
  • Nikkaji Number:J743.395F
  • Wikidata:Q27137103
  • Metabolomics Workbench ID:65171
UDP-N-acetyl-alpha-D-mannosamine

Synonyms:UDP-ManNAc;uridine diphosphate N-acetylmannosamine

Suppliers and Price of UDP-N-acetyl-alpha-D-mannosamine
Supply Marketing:
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
Total 10 raw suppliers
Chemical Property of UDP-N-acetyl-alpha-D-mannosamine
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • PKA:1.10±0.50(Predicted) 
  • Flash Point:°C 
  • PSA:329.23000 
  • Density:1.86g/cm3 
  • LogP:-3.39730 
  • XLogP3:-6.6
  • Hydrogen Bond Donor Count:9
  • Hydrogen Bond Acceptor Count:17
  • Rotatable Bond Count:10
  • Exact Mass:607.08157040
  • Heavy Atom Count:39
  • Complexity:1080
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)NC1C(C(C(OC1OP(=O)(O)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
  • Isomeric SMILES:CC(=O)N[C@H]1[C@H]([C@@H]([C@H](O[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
Technology Process of UDP-N-acetyl-alpha-D-mannosamine

There total 39 articles about UDP-N-acetyl-alpha-D-mannosamine 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:
With yeast inorganic pyrophosphatase; N-acetylglucosamine-1-phosphate pyrophosphorylase from C. jejuni NCTC 11168; tris hydrochloride; magnesium chloride; at 37 ℃; for 2h; pH=7.5;
DOI:10.1016/j.bmcl.2013.06.003
Guidance literature:
With inorganic pyrophosphatase cloned from Pasteurella multocida strain P-1059; N-acetylglucosamine-1-phosphate uridylyltransferase cloned from Pasteurella multocida strain P-1059 (ATCC15742); N-acetylhexosamine 1-kinase cloned from Bifidobacterium longum ATCC55813; ATP; magnesium chloride; In water; at 37 ℃; pH=8; aq. buffer; Enzymatic reaction;
DOI:10.1039/c1cc14034e
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 26575-17-7