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1,1,3,3-Propanetetracarboxylic acid, 2-phenyl-, tetraethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6768-26-9

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6768-26-9 Usage

Chemical Family

Ester

Explanation

The compound belongs to the ester family, which are derived from the reaction between an acid and an alcohol.

Explanation

The ester is formed by the reaction of 2-phenylpropane-1,2,3-tricarboxylic acid with four ethyl alcohol molecules, resulting in the formation of four ester linkages.

Explanation

The molecule consists of a propane chain with a phenyl group (a six-carbon ring) attached at the second carbon, and four carboxylic acid groups attached to the first, second, and third carbons.

Explanation

Due to its high thermal stability and low volatility, the compound is used as a plasticizer to increase the flexibility of plastics and as a lubricant additive to improve the performance of lubricants. It also has potential applications in the pharmaceutical and agricultural industries.

Explanation

It is essential to handle 1,1,3,3-Propanetetracarboxylic acid, 2-phenyl-, tetraethyl ester with care, as it can be harmful if accidentally ingested or inhaled. Additionally, it can cause irritation to the skin and eyes upon contact.

Explanation

The compound exhibits high thermal stability, making it suitable for use in applications that require resistance to high temperatures.

Explanation

The ester has low volatility, which means it does not easily evaporate at room temperature, contributing to its stability in various applications.

Composition

Four ethyl groups and a 2-phenylpropane-1,2,3-tricarboxylic acid molecule

Molecular Structure

2-phenyl group attached to a propane chain with four carboxylic acid groups

Applications

Plasticizer, lubricant additive, pharmaceutical, and agricultural industries

Safety Precautions

Harmful if ingested or inhaled, causes skin and eye irritation

Thermal Stability

High

Volatility

Low

Check Digit Verification of cas no

The CAS Registry Mumber 6768-26-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,6 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6768-26:
(6*6)+(5*7)+(4*6)+(3*8)+(2*2)+(1*6)=129
129 % 10 = 9
So 6768-26-9 is a valid CAS Registry Number.

6768-26-9Relevant academic research and scientific papers

Determination of the electrophilicity parameters of diethyl benzylidenemalonates in dimethyl sulfoxide: Reference electrophiles for characterizing strong nucleophiles

Kaumanns, Oliver,Lucius, Roland,Mayr, Herbert

supporting information; experimental part, p. 9675 - 9682 (2009/09/29)

The second-order rate constants of the reactions of nine substituted diethyl benzylidenemalonates 1a-i with the carbanions 2a-e have been determined spectrophotometrically in dimethyl sulfoxide (DMSO). Product studies show that the nucleophiles attack regioselectively at the electrophilic C=C double bond of the Michael acceptors to form the carbanionic adducts 4. The correlation log k(20°C) = s(N+E) allows the determination of the electrophilicity parameters E for the electrophiles 1a-i from the rate constants determined in this work and the previously published N and s parameters for the nucleophiles 2a-e. The electrophilicities E for compounds 1a-i cover a range of six units (-17.7> E >-23.8) and correlate excellently with Hammett's substituent constants σp. The title compounds are roughly ten orders of magnitude less reactive than analogously substituted benzylidene Meldrum's acids, their cyclic analogues. Due to their low reactivities, compounds 1a-i are suitable reference electrophiles for determining the reactivities of highly reactive nucleophiles, such as carbanions with 16N30.

Tandem Knoevenagel-Michael addition of aryl sulfonimines with diethyl malonate for synthesis of arylidene dimalonates

Fan, Renhua,Wang, Weizi,Pu, Dongming,Wu, Jie

, p. 5905 - 5907 (2008/02/10)

(Chemical Equation Presented) A highly efficient, one-flask tandem Knoevenagel-Michael addition reaction of sulfonimines with diethyl malonate in the presence of a catalytic amount of base affords the corresponding arylidene dimalonates in good to excellent yields.

δ and α SP3 C-H bond oxidation of sulfonamides with PhI(OAc)2/I2 under metal-free conditions

Fan, Renhua,Pu, Dongming,Wen, Fengqi,Wu, Jie

, p. 8994 - 8997 (2008/03/13)

(Chemical Equation Presented) An efficient δ and α sp 3 C-H bond oxidation of sulfonamides with PhI(OAc)2/I 2 under metal-free conditions has been reported. The reaction provides a useful route to pyrrolidines, N-sulfonyli

Synthesis, Screening, and Molecular Modeling of New Potent and Selective Antagonists at the α1d Adrenergic Receptor

Leonardi, Amedeo,Barlocco, Daniela,Montesano, Federica,Cignarella, Giorgio,Motta, Gianni,Testa, Rodolfo,Poggesi, Elena,Seeber, Michele,De Benedetti, Pier G.,Fanelli, Francesca

, p. 1900 - 1918 (2007/10/03)

In the present study, more than 75 compounds structurally related to BMY 7378 have been designed and synthesized. Structural variations of each part of the reference molecule have been introduced, obtaining highly selective ligands for the α1d adrenergic receptor. The molecular determinants for selectivity at this receptor are essentially held by the phenyl substituent in the phenylpiperazine moiety. The integration of an extensive SAR analysis with docking simulations using the rhodopsin-based models of the three α1-AR subtypes and of the 5-HT1A receptor provides significant insights into the characterization of the receptor binding sites as well as into the molecular determinants of ligand selectivity at the α1d-AR and the 5-HT1A receptors. The results of multiple copies simultaneous search (MCSS) on the substituted phenylpiperazines together with those of manual docking of compounds BMY 7378 and 69 into the putative binding sites of the α1a-AR, α1b-AR, α1d-AR, and the 5-HT1A receptors suggest that the phenylpiperazine moiety would dock into a site formed by amino acids in helices 3, 4, 5, 6 and extracellular loop 2 (E2), whereas the spirocyclic ring of the ligand docks into a site formed by amino acids of helices 1, 2, 3, and 7. This docking mode is consistent with the SAR data produced in this work. Furthermore, the binding site of the imide moiety does not allow for the simultaneous involvement of the two carbonyl oxygen atoms in H-bonding interactions, consistent with the SAR data, in particular with the results obtained with the lactam derivative 128. The results of docking simulations also suggest that the second and third extracellular loops may act as selectivity filters for the substituted phenylpiperazines. The most potent and selective compounds for α1d adrenergic receptor, i.e., 69 (Rec 26D/038) and 128 (Rec 26D/073), are characterized by the presence of the 2,5-dichlorophenylpiperazine moiety.

Lewis acidic ionic liquids for the synthesis of electrophilic alkenes via the Knoevenagel condensation

Harjani, Jitendra R,Nara, Susheel J,Salunkhe, Manikrao M

, p. 1127 - 1130 (2007/10/03)

1-Butyl-3-methylimidazolium chloroaluminate, [bmim]Cl·AlCl3, N = 0.67 and 1-butylpyridinium chloroaluminate, [bpy]Cl·AlCl3, N = 0.67 ionic liquids were found to work well as the Lewis acid catalyst and solvent in the Knoevenagel condensations of benzaldehyde and substituted benzaldehydes with diethyl malonate to give benzylidene malonates. The benzylidene malonates subsequently underwent Michael additions with diethyl malonate. The extent of Michael product formed during the reaction was found to vary with the Lewis acidity and the molar proportion of ionic liquid. The influence of Lewis acidity of the ionic liquid on the Knoevenagel and Michael products is demonstrated. In the case of 2-hydroxyarylaldehydes, the reactions led to the formation of 3-ethoxycarbonyl coumarins under ambient conditions.

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