28007-90-1

Basic information

• Product Name: 2-acetamido-2-deoxy-α-D-glucosyl dicyclohexylammonium phosphate
• CAS NO: 28007-90-1
• Molecular Weight: 499.542
• Mol File: 28007-90-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-acetamido-2-deoxy-α-D-glucosyl dicyclohexylammonium phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetamido-2-deoxy-α-D-glucosyl dicyclohexylammonium phosphate(28007-90-1)
• EPA Substance Registry System: 2-acetamido-2-deoxy-α-D-glucosyl dicyclohexylammonium phosphate(28007-90-1)

Safety Data

• Hazardous Substances Data: 28007-90-1(Hazardous Substances Data)

Upstream product

• 3006-60-8 Acetic acid (2R,3R,4R,5S,6R)-2,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-4-yl ester 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 10378-06-0 2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline 
• 108-91-8 cyclohexylamine 
• 79184-08-0 3,4,6-tri-O-acetyl-2-acetamido-1-O-[bis(benzyloxy)phophoryl]-2-deoxy-α-D-glucopyranose 
• 137845-71-7 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucosyl dicyclohexylammonium phosphate 

Relevant articles and documents

Gram-Scale Synthesis of Uridine 5'-Diphospho-N-acetylglucosamine: Comparison of Enzymatic and Chemical Routes

Practical chemoenzymatic and chemical routes to uridine 5'-diphospho-N-acetylglucosamine (UDP-GlcNAc) on a gram scale have been developed.The chemoenzymatic synthesis provided convenient access to glucosamine-6-phosphate and N-acetylglucosamine-6-phosphate (GlcNAc-6-P) in > 10 mmol quantities.The condensation between GlcNAc-6-P and UTP was catalyzed by readily available crude enzyme extract from dried cells of the yeast Candida utilis and afforded a 17 percent yield of UDP-GlcNAc from GlcNAc-6-P.The otherwise straightforward chemoenzymatic sequence was hampered by the need to purify the product from the final complex reaction mixture.The chemical synthesis of UDP-GlcNAc proceeded through five steps in an overall yield of 15 percent from pentaacetylglucosamine with the selective formation of tetraacetylglucosamine-α-1-phosphate as the key reaction.