256382-50-0 Usage
Uses
Used in Organic Synthesis:
(4R)-4-phenyl-3-(1,2-propadienyl)-2-Oxazolidinone is used as a building block in organic synthesis for the creation of other complex compounds. Its unique structure and functional groups contribute to the synthesis of a variety of organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4R)-4-phenyl-3-(1,2-propadienyl)-2-Oxazolidinone is used as a pharmacophore for drug discovery. Its complex structure and stereochemistry may offer potential in the development of new pharmaceutical agents.
Used in Pharmaceutical Industry:
(4R)-4-phenyl-3-(1,2-propadienyl)-2-Oxazolidinone is used as a precursor in the pharmaceutical industry for the synthesis of drugs with potential therapeutic applications. Its unique structural features may contribute to the discovery of novel medications.
Used in Research and Development:
(4R)-4-phenyl-3-(1,2-propadienyl)-2-Oxazolidinone is utilized in research and development settings to explore its properties and potential applications. Its reactivity and biological activity are of interest to scientists working on new chemical and pharmaceutical innovations.
Check Digit Verification of cas no
The CAS Registry Mumber 256382-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,3,8 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 256382-50:
(8*2)+(7*5)+(6*6)+(5*3)+(4*8)+(3*2)+(2*5)+(1*0)=150
150 % 10 = 0
So 256382-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO2/c1-2-8-13-11(9-15-12(13)14)10-6-4-3-5-7-10/h3-8,11H,1,9H2/t11-/m0/s1
256382-50-0Relevant academic research and scientific papers
Efficient preparations of novel ynamides and allenamides
Wei, Lin-Li,Mulder, Jason A.,Xiong, Hui,Zificsak, Craig A.,Douglas, Christopher J.,Hsung, Richard P.
, p. 459 - 466 (2007/10/03)
Practical syntheses of a series of novel ynamides and allenamides are described here. While a base-induced isomerization protocol of propargyl amides leads to an array of chiral and achiral allenamides, ynamides are prepared from enamides via bromination followed by base-induced elimination of the Z-bromoenamides. These ynamides and allenamides possess improved thermal stability compared to ynamines and allenamines. They can be isolated, purified, and handled with ease, and thus, should be synthetically more useful than traditional ynamines and allenamines.
First stereoselective inverse demand [4 + 2] cycloaddition reactions of novel chiral allenamides with heterodienes. Preparation of highly functionalized 2-arylpyranyl heterocycles
Wei, Lin-Li,Hsung, Richard P.,Xiong, Hui,Mulder, Jason A.,Nkansah, Nancy T.
, p. 2145 - 2148 (2008/02/09)
matrix presented The first stereoselective inverse demand [4 + 2] cycloaddition reactions of chiral allenamides with heterodienes are described here. These reactions lead to stereoselective synthesis of highly functionalized pyranyl heterocycles. A mechan
