256382-50-0 Usage
General Description
(4R)-4-phenyl-3-(1,2-propadienyl)-2-Oxazolidinone is a chemical compound with a unique structure and properties. It is an oxazolidinone derivative with a four-membered ring containing oxygen and nitrogen atoms. The compound has a phenyl group and a 1,2-propadienyl group attached to the oxazolidinone ring, giving it a complex and potentially useful structure for various applications in organic synthesis and medicinal chemistry. (4R)-4-phenyl-3-(1,2-propadienyl)-2-Oxazolidinone may have potential as a building block for the synthesis of other compounds or as a pharmacophore for drug discovery. Additionally, its stereochemistry as (4R) may also play a role in its reactivity and biological activity. Overall, (4R)-4-phenyl-3-(1,2-propadienyl)-2-Oxazolidinone is an interesting and potentially valuable chemical compound with diverse potential applications.
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 articles and documents
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.
