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5-phenyl-2-phenylimino-3-methyl-4-oxazolidinone is a complex organic compound with the molecular formula C17H14N2O2. It is a derivative of oxazolidinone, a heterocyclic compound containing oxygen, nitrogen, and carbon atoms. The structure of 5-phenyl-2-phenylimino-3-methyl-4-oxazolidinone features a five-membered oxazolidinone ring with a methyl group at the 3-position, a phenyl group at the 5-position, and a phenylimino group at the 2-position. 5-phenyl-2-phenylimino-3-methyl-4-oxazolidinone is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and reactivity. However, further research and characterization are needed to fully understand its properties and potential uses.

5841-17-8

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5841-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5841-17-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5841-17:
(6*5)+(5*8)+(4*4)+(3*1)+(2*1)+(1*7)=98
98 % 10 = 8
So 5841-17-8 is a valid CAS Registry Number.

5841-17-8Downstream Products

5841-17-8Relevant academic research and scientific papers

STRUCTURE AND DUAL REACTIVITY OF 2-PHENYLPEMOLINE

Ramsh, S. M.,Khrabrova, E. S.,Ginak, A. I.

, p. 325 - 329 (2007/10/02)

5-Phenyl-2-phenylimino-4-oxazolidinone exists in DMSO-D6 in the form of a mixture of the E and Z isomers of the imino tautomer, but it crystallizes in the amino form.Parallelism between the basicity and nucleophilicity of the reaction centers of this mesomeric anion is observed when the alternative isomers (and the tautomers corresponding to them) differ significantly in stability.If this condition is not fulfilled, these parameters do not coincide, as is illustrated in the example of its methylation reaction.

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