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5-phenyl-2-methylphenylamino-4-oxazolinone is a complex organic compound with the molecular formula C17H16N2O2. It is characterized by a phenyl group (C6H5) attached to the 5-position of the oxazolinone ring, a methyl group (CH3) at the 2-position, and an amino group (NH2) connected to a phenyl ring at the 4-position. 5-phenyl-2-methylphenylamino-4-oxazolinone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is also of interest in the field of materials science for its potential use in the development of new polymers and other advanced materials. The compound's properties, such as its stability and solubility, make it a valuable intermediate in organic synthesis.

5841-16-7

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5841-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5841-16-7 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 5841-16:
(6*5)+(5*8)+(4*4)+(3*1)+(2*1)+(1*6)=97
97 % 10 = 7
So 5841-16-7 is a valid CAS Registry Number.

5841-16-7Downstream Products

5841-16-7Relevant academic research and scientific papers

STRUCTURE AND DUAL REACTIVITY OF 2-PHENYLPEMOLINE

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

, p. 325 - 329 (1989)

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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