34693-23-7 Usage
Uses
Used in Pharmaceutical Applications:
[2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid is used as a potential therapeutic agent for various medical conditions due to its unique structure and properties. Its phosphonic acid group may offer advantages in targeting specific biological processes, making it a candidate for drug development and treatment of certain diseases.
Used in Agricultural Applications:
In the agricultural industry, [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid may be utilized as a component in the development of novel pesticides or fertilizers. Its complex structure could provide new ways to enhance crop yield, protect plants from pests, or improve nutrient uptake.
Used in Materials Science:
[2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid's unique chemical structure may also find applications in materials science. It could be used in the development of new materials with specific properties, such as improved strength, durability, or chemical resistance, depending on the needs of various industries.
Further research and exploration of [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid are necessary to fully understand its potential uses and benefits across these industries. As our knowledge of [2,3,4-trihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methoxyphosphonic acid grows, so too will the range of applications it can be utilized in.
Check Digit Verification of cas no
The CAS Registry Mumber 34693-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,9 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34693-23:
(7*3)+(6*4)+(5*6)+(4*9)+(3*3)+(2*2)+(1*3)=127
127 % 10 = 7
So 34693-23-7 is a valid CAS Registry Number.
34693-23-7Relevant academic research and scientific papers
Anomerization of Furanose Sugars and Sugar Phosphates
Pierce, John,Serianni, Anthony S.,Barker, Robert
, p. 2448 - 2456 (2007/10/02)
Thermodynamic and kinetic parameters for the ring-opening and -closing reactions of several aldo- and ketofuanoses and their phosphate esters have been determined by NMR line-width and saturation-transfer methods.Cyclic forms interconvert via a single, acyclic carbonyl form under either acid or base catalysis.Ring-opening rates do not correlate with thermodynamic stability of the rings.For aldofuranose phosphates, α anomers open faster than β anomers; for ketofuranose phosphates the converse is observed.Intramolecular catalysis of anomerization by the phosphate group of sugar phosphates is documented.Biological and mechanistic implications of the observed kinetics are discussed.
Synthesis of Sugars by Aldolase-Catalyzed Condensation Reactions
Wong, Chi-Huey,Whitesides, George M.
, p. 3199 - 3205 (2007/10/02)
Dihydroxyacetone phosphate was prepared in 200-mmol scale from dihydroxyacetone by two procedures: reaction with phosphorus oxytrichloride and glycerol kinase catalyzed phosphorylation using ATP with in situ regeneration of ATP by phosphoenolpyruvate or acetyl phosphate.Dihydroxyacetone phosphate was converted to fructose 6-phosphate in 80percent yield by exposure to a mixture of co-immobilized triosephosphate isomerase and aldolase followed by acid hydrolysis of the condensation product fructose 1,6-bisphosphate.Fructose 6-phosphate was subsequently converted by chemical and enzymatic schemes into fructose, glucose 6-phosphate, and glucose.Practical procedures are described for the preparation of D- and L-glyceraldehyde 3-phosphate and for several hexoses labeled with 13C in the C-2 and C-2,5 positions.
