89291-71-4 Usage
General Description
DiMethyl 2-((4R,5R)-5-((R)-2-(benzyloxy)-1-hydroxyethyl)-2,2-diMethyl-1,3-dioxolan-4-yl)-2-oxoethylphosphonate is a chemical compound with a complex molecular structure. It contains a dioxolan ring and a phosphonate group, as well as a benzyloxy and hydroxyethyl side chain. diMethyl 2-((4R,5R)-5-((R)-2-(benzyloxy)-1-hydroxyethyl)-2,2-diMethyl-1,3-dioxolan-4-yl)-2-oxoethylphosphonate is a diMethyl ester and has a 2-oxoethyl group, adding to its complexity. The presence of chiral centers indicates that this compound can exist as enantiomers, each with different properties. Due to its intricate structure, diMethyl 2-((4R,5R)-5-((R)-2-(benzyloxy)-1-hydroxyethyl)-2,2-diMethyl-1,3-dioxolan-4-yl)-2-oxoethylphosphonate likely has potential applications in organic synthesis, pharmaceuticals, or material science. However, further research and analysis are needed to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 89291-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,9 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89291-71:
(7*8)+(6*9)+(5*2)+(4*9)+(3*1)+(2*7)+(1*1)=174
174 % 10 = 4
So 89291-71-4 is a valid CAS Registry Number.
89291-71-4Relevant articles and documents
First synthesis of (-)-neplanocin C
Comin, María J.,Rodriguez, Juan B.
, p. 4639 - 4649 (2007/10/03)
(-)-Neplanocin C (4), a minor component of the neplanocin family of antibiotics and a lead drug for the design of several conformationally constrained nucleosides analogues, was enantioselectively synthesized starting from D-ribono-1,4-lactone via a convergent approach in twelve steps. The proton NMR spectrum of 4 was in agreement with the corresponding natural product. Calculated coupling constants obtained from ab initio molecular modeling studies and from previously published X-ray structure of neplanocin C also corresponded to the spectroscopic data. (C) 2000 Elsevier Science Ltd.
CONVENIENT OXIDATIONS OF CARBOHYDRATE DERIVED LACTOLS AND OF ε-HYDROXY-β-KETOPHOSPHONATES
Csuk, Rene,Doerr, Petra
, p. 35 - 44 (2007/10/02)
Convenient oxidation of carbohydrate derived lactols to lactones as well as the oxidation of ε-hydroxy-β-ketophosphonates to their corresponding β,ε-diketophosphonates can be performed with the Dess-Martin periodinane in high yields.
TOTAL SYNTHESIS OF (-)-NEPLANOCIN A
Lim, Mu-ill,Marquez, Victor E.
, p. 5559 - 5562 (2007/10/02)
A total synthesis of (-)-neplanocin A has been accomplished in 15 steps starting from the readily available D-(+)-ribonic acid γ-lactone.