58865-20-6 Usage
Description
α-d-galacturonic acid 1-phosphate lithium salt is an uronic acid phosphate derived from alpha-D-galacturonic acid, which carries a phosphate group at position 1. It is a compound with potential applications in various industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
α-d-galacturonic acid 1-phosphate lithium salt is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: α-d-galacturonic acid 1-phosphate lithium salt is used as a therapeutic agent for its ability to modulate various biological pathways and exhibit potential health benefits.
Used in Chemical Synthesis:
In the chemical industry, α-d-galacturonic acid 1-phosphate lithium salt is used as a key intermediate in the synthesis of various complex organic compounds. The expression is: α-d-galacturonic acid 1-phosphate lithium salt is used as a synthetic intermediate for its role in creating a wide range of chemical products.
Used in Research and Development:
α-d-galacturonic acid 1-phosphate lithium salt is utilized in research and development as a valuable tool for studying the structure and function of biological molecules. The expression is: α-d-galacturonic acid 1-phosphate lithium salt is used as a research tool for its contribution to the understanding of molecular interactions and biological processes.
Used in Food Industry:
In the food industry, α-d-galacturonic acid 1-phosphate lithium salt may be used as an additive or ingredient in the development of novel food products. The expression is: α-d-galacturonic acid 1-phosphate lithium salt is used as a food additive for its potential to enhance the properties and quality of various food items.
Check Digit Verification of cas no
The CAS Registry Mumber 58865-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,6 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58865-20:
(7*5)+(6*8)+(5*8)+(4*6)+(3*5)+(2*2)+(1*0)=166
166 % 10 = 6
So 58865-20-6 is a valid CAS Registry Number.
58865-20-6Relevant articles and documents
Improved one-pot multienzyme (OPME) systems for synthesizing UDP-uronic acids and glucuronides
Muthana, Musleh M.,Qu, Jingyao,Xue, Mengyang,Klyuchnik, Timofey,Siu, Alex,Li, Yanhong,Zhang, Lei,Yu, Hai,Li, Lei,Wang, Peng G.,Chen, Xi
supporting information, p. 4595 - 4598 (2015/05/27)
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
CHEMOENZYMATIC SYNTHESIS OF HEPARIN AND HEPARAN SULFATE ANALOGS
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Paragraph 0337; 0338; 0339; 0340, (2014/09/03)
The present invention provides a one-pot multi-enzyme method for preparing UDP-sugars from simple sugar starting materials. The invention also provides a one-pot multi-enzyme method for preparing oligosaccharides from simple sugar starting materials.
Process for selective oxidation of primary alcohols
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, (2008/06/13)
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.
