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5-(4-chloro-benzyl)-5-phenyl-imidazolidine-2,4-dione is a complex organic compound with the molecular formula C16H13ClN2O2. It features a central imidazolidine-2,4-dione ring, which is a five-membered ring containing two oxygen atoms and two nitrogen atoms. The compound is characterized by a 4-chloro-benzyl group attached to the 5-position of the imidazolidine ring, which introduces a chlorine atom to the structure. Additionally, a phenyl group is also attached to the same 5-position, further enhancing the molecular complexity. This chemical is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various biologically active molecules. Its specific properties, such as solubility and reactivity, can be influenced by the presence of the chlorine atom and the phenyl group, making it a compound of interest in organic chemistry and drug development.

6332-85-0

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6332-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6332-85-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6332-85:
(6*6)+(5*3)+(4*3)+(3*2)+(2*8)+(1*5)=90
90 % 10 = 0
So 6332-85-0 is a valid CAS Registry Number.

6332-85-0Relevant academic research and scientific papers

Efficient synthesis of 5-arylmethyl-5-phenylimidazolidine-2,4-dione (or 5-arylmethyl-5-phenyl-2-thioxoimidazolidin-4-one) from chalcone oxides under ultrasound irradiation

Li, Ji-Tai,Xu, Xiao-Ya,Yin, Ying

experimental part, p. 198 - 201 (2012/04/04)

Synthesis of 5-arylmetlryl-5-phenylirnidazolidine-2,4-dione (or 5-arylmethyl-5-phenyl-2-thoxoimidazolidin-4- one) via the reaction of 3-aryl-2,3-epoxyl-1-phenyl-1-propanone and urea (or thiourea) was carried out in 57-98% yields at 50 °C in EtOH in the pr

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 (2008/02/11)

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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