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2,4-Imidazolidinedione, 5-(4-methoxyphenyl)-5-(phenylmethyl)-, also known as 5-(4-methoxyphenyl)-5-(phenylmethyl)imidazolidine-2,4-dione, is a chemical compound with the molecular formula C16H15NO3. It is a white crystalline solid that is soluble in organic solvents. 2,4-Imidazolidinedione, 5-(4-methoxyphenyl)-5-(phenylmethyl)- is a derivative of imidazolidinedione, which is a heterocyclic compound with a five-membered ring containing two nitrogen atoms and one oxygen atom. The 5-(4-methoxyphenyl)-5-(phenylmethyl) substitution pattern indicates the presence of a 4-methoxyphenyl group and a phenylmethyl group attached to the imidazolidinedione core. This specific chemical structure may have potential applications in pharmaceuticals, agrochemicals, or other industrial settings, although its specific uses and properties would depend on further research and development.

4927-44-0

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4927-44-0 Usage

General Description

2,4-Imidazolidinedione, 5-(4-methoxyphenyl)-5-(phenylmethyl)- is a chemical compound with the molecular formula C17H18N2O3. It is a derivative of imidazolidinedione and contains a 4-methoxyphenyl and a phenylmethyl group. 2,4-Imidazolidinedione, 5-(4-methoxyphenyl)-5-(phenylmethyl)- is known for its potential anticonvulsant and antiviral properties. It has been studied for its potential use in the treatment of epilepsy and other neurological disorders, as well as for its ability to inhibit the replication of certain viruses. However, further research is needed to fully understand its biological effects and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4927-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4927-44:
(6*4)+(5*9)+(4*2)+(3*7)+(2*4)+(1*4)=110
110 % 10 = 0
So 4927-44-0 is a valid CAS Registry Number.

4927-44-0Downstream Products

4927-44-0Relevant articles and documents

A novel one-pot rearrangement reaction of 2,3-epoxydiaryl ketones: Synthesis of (±)-5,5-disubstituted imidazolones and 5,5-disubstituted hydantoins

Bhat, Bilal A.,Dhar, Kanaya L.,Puri, Satish C.,Spiteller, Michael

, p. 2723 - 2726 (2006)

A novel one-pot rearrangement reaction, involving sequential epoxide rearrangement, condensation, cyclization and phenyl migration took place when 2,3-epoxydiphenyl ketones were treated with guanidine hydrochloride or urea in the presence of a base like s

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