6920-57-6

Basic information

• Product Name: α-D-Glucuronsaeure-1-phosphat
• CAS NO: 6920-57-6
• Molecular Weight: 274.121
• Mol File: 6920-57-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: α-D-Glucuronsaeure-1-phosphat(CAS DataBase Reference)
• NIST Chemistry Reference: α-D-Glucuronsaeure-1-phosphat(6920-57-6)
• EPA Substance Registry System: α-D-Glucuronsaeure-1-phosphat(6920-57-6)

Safety Data

• Hazardous Substances Data: 6920-57-6(Hazardous Substances Data)

Upstream product

• 6556-12-3 D-glucuronic acid 

Downstream Products

• 2616-64-0 UDP-glucuronic acid 
• 32449-92-6 D-glucurono-6,3-lactone 

Relevant articles and documents

Improved one-pot multienzyme (OPME) systems for synthesizing UDP-uronic acids and glucuronides

Arabidopsis thaliana glucuronokinase (AtGlcAK) was cloned and shown to be able to use various uronic acids as substrates to produce the corresponding uronic acid-1-phosphates. AtGlcAK or Bifidobacterium infantis galactokinase (BiGalK) was used with a UDP-sugar pyrophosphorylase, an inorganic pyrophosphatase, with or without a glycosyltransferase for highly efficient synthesis of UDP-uronic acids and glucuronides. These improved cost-effective one-pot multienzyme (OPME) systems avoid the use of nicotinamide adenine dinucleotide (NAD+)-cofactor in dehydrogenase-dependent UDP-glucuronic acid production processes and can be broadly applied for synthesizing various glucuronic acid-containing molecules. This journal is

Process for selective oxidation of primary alcohols

Primary alcohols, especially in carbohydrates, can be selectively oxidized to aldehydes and carboxylic acids in a low-halogen process by using a peracid in the presence of a catalytic amount of a di-tertiary-alkyl nitroxyl (TEMPO) and a catalytic amount of halide. The halide is preferably bromide and the process can be carried out at nearly neutral to moderately alkaline pH (5-11). The peracid can be produced or regenerated by means of hydrogen peroxide or oxygen. The process is advantageous for producing uronic acids and for introducing aldehyde groups which are suitable for crosslinking and derivatization.