89539-47-9 Usage
Molecular Structure
Contains a pyrrolidinedione ring structure and a phenylimino functional group.
Physical State
Pale yellow solid.
Use in Organic Synthesis
Commonly utilized in organic synthesis due to its reactivity and versatility.
Application in Pharmaceutical Research
Often employed in pharmaceutical research due to its potential medicinal properties.
(Z)Configuration
Indicates a cis configuration around the double bond in the phenylimino group.
Potential Drug Development
May have potential applications in the development of new drugs.
Possible Use in Specialty Chemical Production
Due to its unique structure and properties, it might find application in the production of specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 89539-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89539-47:
(7*8)+(6*9)+(5*5)+(4*3)+(3*9)+(2*4)+(1*7)=189
189 % 10 = 9
So 89539-47-9 is a valid CAS Registry Number.
89539-47-9Relevant articles and documents
C-SUBSTITUTION REACTIONS OF C,N-DIARYL NITRONES.
Lobo, Ana M.,Prabhakar, Sundaresan,Rzepa, Henry S.,Skapski, Andrzej C.,Tavares, M. Regina,Widdowson, David A.
, p. 3833 - 3842 (2007/10/02)
C,N-Diaryl nitrones react rapidly with N-bromosuccinimide in an aprotic solvent to yield among other products, the E and Z isomers of the C-succinimidyl substituted nitrones and a small amount of the corresponding hydroxamic acid.The sterochemistry of the C-succinimidyl niyrones was confirmed by an X-ray structure determination of the C,N-(dimethoxyphenyl) derivative 8e.In the presence of the base DABCO the formation of hydroxamic acids is suppressed and the Z C-succinimidyl nitrone forms more rapidly than the more stable E isomer.Several mechanistic rationalisations of this observed stereochemistry are discussed.
