4212-65-1 Usage
Description
(2,3,5-trihydroxy-4-oxo-pentoxy)phosphonic acid is a complex organic compound with a unique structure that features three hydroxyl groups and a phosphonic acid group attached to a pentoxy ring. This molecule is characterized by its ability to form strong hydrogen bonds and coordinate with metal ions, making it a versatile compound with potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(2,3,5-trihydroxy-4-oxo-pentoxy)phosphonic acid is used as a chelating agent for metal ions in pharmaceutical formulations. Its ability to form stable complexes with metal ions helps to improve the solubility, stability, and bioavailability of metal-based drugs, such as those containing iron, zinc, or copper.
Used in Chemical Synthesis:
(2,3,5-trihydroxy-4-oxo-pentoxy)phosphonic acid is used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and functional groups make it a valuable intermediate in the development of new molecules with specific properties and applications.
Used in Environmental Remediation:
(2,3,5-trihydroxy-4-oxo-pentoxy)phosphonic acid is used as a sequestering agent for metal ions in wastewater treatment and environmental remediation processes. Its ability to form stable complexes with metal ions helps to remove toxic metals from contaminated water and soil, reducing their environmental impact and improving the quality of the ecosystem.
Used in Analytical Chemistry:
(2,3,5-trihydroxy-4-oxo-pentoxy)phosphonic acid is used as a reagent in analytical chemistry for the detection and quantification of metal ions. Its strong affinity for metal ions allows for the development of sensitive and selective assays, which can be used to monitor metal ion concentrations in various samples, such as water, soil, and biological tissues.
Used in Material Science:
(2,3,5-trihydroxy-4-oxo-pentoxy)phosphonic acid is used as a functionalizing agent in the development of advanced materials, such as metal-organic frameworks (MOFs), coordination polymers, and hybrid materials. Its ability to form strong coordination bonds with metal ions enables the design of materials with tailored properties, such as high porosity, selectivity, and catalytic activity, for applications in gas storage, separation, and catalysis.
Check Digit Verification of cas no
The CAS Registry Mumber 4212-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,1 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4212-65:
(6*4)+(5*2)+(4*1)+(3*2)+(2*6)+(1*5)=61
61 % 10 = 1
So 4212-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H11O8P/c6-1-3(7)5(9)4(8)2-13-14(10,11)12/h4-6,8-9H,1-2H2,(H2,10,11,12)/t4-,5-/m1/s1
4212-65-1Relevant articles and documents
Chemical Synthesis of Ketopentose-5-phosphates
Wei, Wei-Chih,Chang, Che-Chien
, p. 3033 - 3040 (2017/06/20)
A chemical synthesis of ketopentose-5-phosphates that are involved in the pentose phosphate pathway has been developed. The ketopentose phosphates, d-ribulose-5-phosphate and d-xylulose-5-phosphate, were prepared in five steps starting from known intermed
Synthesis of arabinitol 1-phosphate and its use for characterization of arabinitol-phosphate dehydrogenase
Soroka, Nikolai V.,Kulminskaya, Anna A.,Eneyskaya, Elena V.,Shabalin, Konstantin A.,Uffimtcev, Andrei V.,Povelainen, Mira,Miasnikov, Andrei N.,Neustroev, Kirill N.
, p. 539 - 546 (2007/10/03)
D-Arabinitol 1-phosphate (Ara-ol1-P), a substrate for d-arabinitol- phosphate dehydrogenase (APDH), was chemically synthesized from d-arabinonic acid in five steps (O-acetylation, chlorination, reduction, phosphorylation, and de-O-acetylation). Ara-ol1-P was used as a substrate for the characterization of APDH from Bacillus halodurans. APDH converts Ara-ol1-P to xylulose 5-phosphate in the oxidative reaction; both NAD+ and NADP+ were accepted as co-factors. Kinetic parameters for the oxidative and reductive reactions are consistent with a ternary complex mechanism.
UTILIZATION OF ENZYMES IN ORGANIC CHEMISTRY : TRANSKETOLASE CATALYZED SYNTHESIS OF KETOSES
Bolte, Jean,Demdynck, Colette,Samaki, Hamid
, p. 5525 - 5528 (2007/10/02)
Substrate specificity of bakers' yeast transketolase has been studied: the enzyme appears to be enantioselective towards the acceptor aldehyde.L-erythrulose, D-xylulose and 5-deoxy-D-xylulose have been synthesized by spinach transketolase catalyzed condensation of hydroxypyruvate and the corresponding aldehyde.
