178327-18-9 Usage
Description
[3(1R,2R),4S]-4-benzyl-3-(2-hydroxycyclopent-3-enecarbonyl)oxazolidin-2-one is a complex chemical compound belonging to the class of oxazolidinones, which are heterocyclic compounds characterized by a five-membered ring containing both oxygen and nitrogen atoms. This specific compound features a benzyl group and a hydroxycyclopentene carbonyl group, which are significant functional groups in the realm of organic chemistry. The stereochemistry of the molecule is defined by the R and S configurations, detailing the spatial arrangement of the substituent groups around the chiral centers.
Uses
Used in Medicinal Chemistry:
[3(1R,2R),4S]-4-benzyl-3-(2-hydroxycyclopent-3-enecarbonyl)oxazolidin-2-one is used as a potential candidate in medicinal chemistry due to its unique structure and functional groups. [3(1R,2R),4S]-4-benzyl-3-(2-hydroxycyclopent-3-enecarbonyl)oxazolidin-2-one's specific stereochemistry and the presence of a benzyl and hydroxycyclopentene carbonyl group may contribute to its interaction with biological targets, making it a promising candidate for the development of new drugs or therapeutic agents.
Used as a Synthetic Intermediate in Organic Synthesis:
In the field of organic synthesis, [3(1R,2R),4S]-4-benzyl-3-(2-hydroxycyclopent-3-enecarbonyl)oxazolidin-2-one can be utilized as a synthetic intermediate. Its complex structure and functional groups make it a valuable building block for the creation of more complex molecules, which could be applied in various industries, such as pharmaceuticals, agrochemicals, or materials science.
Used in Pharmaceutical Industry:
[3(1R,2R),4S]-4-benzyl-3-(2-hydroxycyclopent-3-enecarbonyl)oxazolidin-2-one is used as a potential therapeutic agent in the pharmaceutical industry. Its unique structure and stereochemistry may allow it to target specific biological pathways or receptors, potentially leading to the development of new treatments for various diseases and conditions.
Used in Chemical Research:
In the field of chemical research, [3(1R,2R),4S]-4-benzyl-3-(2-hydroxycyclopent-3-enecarbonyl)oxazolidin-2-one can serve as a valuable compound for studying the properties and reactivity of oxazolidinones and related heterocyclic compounds. This may lead to a better understanding of their potential applications and the development of new synthetic methods or strategies for their preparation.
Check Digit Verification of cas no
The CAS Registry Mumber 178327-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,3,2 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 178327-18:
(8*1)+(7*7)+(6*8)+(5*3)+(4*2)+(3*7)+(2*1)+(1*8)=159
159 % 10 = 9
So 178327-18-9 is a valid CAS Registry Number.
178327-18-9Relevant articles and documents
An efficient, general asymmetric synthesis of carbocyclic nucleosides: Application of an asymmetric aldol/ring-closing metathesis strategy
Crimmins,King,Zuercher,Choy
, p. 8499 - 8509 (2007/10/03)
A general and efficient synthesis of carbocyclic and hexenopyranosyl nucleosides has been developed. The strategy combines three key transformations: an asymmetric aldol addition to establish the relative and absolute configuration of the pseudosugar, a ring-closing metathesis to construct the pseudosugar ring, and a Trost-type palladium(0)-mediated substitution to assemble the pseudosugar and the aromatic base. Carbovir, abacavir, and their 2'-methyl derivatives as well as hexenopyranosyl nucleoside analogues have been prepared by this sequence.
