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5,5-diphenyl-3-(prop-2-yn-1-yl)imidazolidine-2,4-dione is a complex organic compound with the molecular formula C18H15N2O2. It is characterized by a central imidazolidine-2,4-dione ring, which is a five-membered ring containing two carbonyl groups (C=O) at the 2 and 4 positions. The molecule features two phenyl groups (C6H5) attached to the 5 position of the imidazolidine ring, and a prop-2-yn-1-yl group (a propargyl group, which is a three-carbon chain with a triple bond at one end) attached to the 3 position. 5,5-diphenyl-3-(prop-2-yn-1-yl)imidazolidine-2,4-dione is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, due to its unique structure and reactivity.

2718-07-2

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2718-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2718-07-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2718-07:
(6*2)+(5*7)+(4*1)+(3*8)+(2*0)+(1*7)=82
82 % 10 = 2
So 2718-07-2 is a valid CAS Registry Number.

2718-07-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-diphenyl-3-prop-2-ynylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-Imidazolidinedione,5,5-diphenyl-3-(2-propynyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2718-07-2 SDS

2718-07-2Relevant academic research and scientific papers

Anticonvulsant activity of reaction products of 5,5-diphenylhydantoin with substituted methylene bromides

Usifoh, Cyril O.

, p. 366 - 368 (2001)

Some derivatives of 5,5-diphenylhydantoin (phenytoin) were synthesized by the alkylation of phenytoin with substituted methylene bromides. The hydantoins were evaluated for possible anticonvulsant activity in the maximal electroshock (MES)- and subcutaneous pentylenetetrazole (ScMet)-induced seizures and for neurotoxicity in the rotorod test in mice and rats.

Synthesis of hydantoin alkynes through palladium-catalyzed reaction, antibacterial evaluation, and molecular docking studies

Keivanloo, Ali,Lashkari, Saeed,Sepehri, Saghi,Bakherad, Mohammad,Abbaspour, Sima

, p. 1317 - 1327 (2021)

Novel 3-(3-(aryl)prop-2-yn-1-yl)-5,5-diphenylimidazolidine-2,4-diones were synthesized through the reaction of 5,5-diphenyl-3-(prop-2-yn-1-yl)imidazolidine-2,4-dione and aryl iodides in the presence of a palladium-copper catalytic in CH3CN at r

Ligand-assisted click reaction for the synthesis of new hybrid compounds based on 1,2,3-triazoles and 5,5-diphenylimidazolidine-2,4-dione and evaluation of their antibacterial activities

Keivanloo, Ali,Lashkari, Saeed,Sepehri, Saghi,Bakherad, Mohammad,Abbaspour, Sima

, p. 935 - 943 (2020/05/29)

The new hybrid compounds based on 1,2,3-triazoles and 5,5-diphenylimidazolidine-2,4-dione were successfully synthesized by copper-catalyzed click reaction in the presence of water-soluble ligand, sodium 4-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate and

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