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methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside

Base Information Edit
  • Chemical Name:methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside
  • CAS No.:73448-32-5
  • Molecular Formula:C24H31NO13
  • Molecular Weight:541.509
  • Hs Code.:
  • Mol file:73448-32-5.mol
methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside

Synonyms:methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside

Suppliers and Price of methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside
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
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Total 5 raw suppliers
Chemical Property of methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:917.8°C at 760 mmHg 
  • Flash Point:508.9°C 
  • Density:1.58g/cm3 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
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MSDS Files:
Useful:
Technology Process of methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside

There total 6 articles about methylumbelliferyl 2-acetamido-2-deoxy-beta-D-lactoside 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 bovine β-(1 ->; -galactosyltransferase; magnesium chloride; alkaline phosphatase; benzenesulfonamide; In various solvent(s); at 37 ℃; for 48h; pH=7.0;
DOI:10.1016/j.carres.2004.03.015
Guidance literature:
With E. coli K-12 Glc-1-P uridylyltransferase; E. coli UDP-galactose-4-epimerase; Neisseria meningitidis β1-4-galactosyltransferase encoded by lgtB gene; Pasteurella multocida inorganic pyrophosphatase; uridine 5’-(hydrogen triphosphate); magnesium chloride; at 37 ℃; pH=7.5; regioselective reaction; aq. buffer; Enzymatic reaction;
DOI:10.1039/c0cc01381a
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