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1-(furan-2-ylmethyl)-4-[hydroxy(4-methylphenyl)methylidene]-5-(thiophen-2-yl)pyrrolidine-2,3-dione is a complex organic compound with a molecular formula of C20H17NO3S2. It is characterized by a pyrrolidine-2,3-dione core, which is a heterocyclic ring containing two carbonyl groups. The compound features a furan-2-ylmethyl group attached to the nitrogen atom, a hydroxy(4-methylphenyl)methylidene moiety that acts as a bridge between the pyrrolidine ring and a thiophene ring. The presence of both aromatic and heterocyclic rings, as well as the functional groups like hydroxyl and carbonyl, suggests that 1-(furan-2-ylmethyl)-4-[hydroxy(4-methylphenyl)methylidene]-5-(thiophen-2-yl)pyrrolidine-2,3-dione may have unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

4824-74-2

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4824-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4824-74-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,2 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4824-74:
(6*4)+(5*8)+(4*2)+(3*4)+(2*7)+(1*4)=102
102 % 10 = 2
So 4824-74-2 is a valid CAS Registry Number.

4824-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(furan-2-ylmethyl)-4-[hydroxy-(4-methylphenyl)methylidene]-5-thiophen-2-ylpyrrolidine-2,3-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:4824-74-2 SDS

4824-74-2Downstream Products

4824-74-2Relevant academic research and scientific papers

Study on the reaction between bisphenol A and dimethyl carbonate over organotin oxide

He, Xiaolong,Li, Zhenhuan,Su, Kunmei,Cheng, Bowen,Ming, Jun

, p. 20 - 23 (2013/05/09)

Organotin oxide was used to catalyze the reaction between BPA (bisphenol A) and DMC (dimethyl carbonate), and Ph2SnO (diphenyltin oxide) displays the excellent catalytic performance in transesterification and O-methylation. However, Bu2SnO (dibutyltin oxide), (PhCH 2)2SnO (dibenzyltin oxide) and (C6H 11)2SnO (dicyclohexyltin oxide) exhibited weaker catalytic activity but higher selectivity for C-methylation product formation. The π-π function between Ph2SnO and BPA provided more chances for their interaction, and π-d interaction between phenyl ring and Sn resulted in catalyst having higher activity in transesterification and O-methylation. O-methylation product formation over Ph2SnO comes from transesterification product decomposition not from direct methylation of BPA with DMC.

Studies on the carboxymethylation and methylation of bisphenol A with dimethyl carbonate over TiO2/SBA-15

Su, Kunmei,Li, Zhenhuan,Cheng, Bowen,liao, Kun,Shen, Dexin,Wang, Yufei

experimental part, p. 60 - 68 (2010/04/25)

Carboxymethylated species were selectively synthesized from dimethyl carbonate (DMC) and bisphenol A (BPA) over TiO2/SBA-15. On the basis of catalyst characterization by means of XRD, FT-IR, HPLC and GC-MS, the relations between catalytic performance and catalyst properties were discussed. Si-O-Ti was active sites for reaction, and the interaction mode between Ti-O-Si and DMC was main factor to determine carboxymethylation and methylation. When DMC was attacked by Ti-O-Si on two oxygen atoms of CH3-O moiety, BPA attacked carbonyl carbon to form carboxymethylated products. If the interaction occurs through the oxygen of C{double bond, long}O moiety, BPA attacked methyl carbon to form methylated products. Chemisorbed H2O over TiO2/SBA-15 made DMC to act as methylating agent. After chemisorbed H2O was removed, carboxymethylated species of two-methylcarbonate-ended-BPA (DmC(1)) and one-methylcarbonate-ended-BPA (MmC(1)) were selectively synthesized.

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