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diethyl 2-(4-(dimethylamino)phenyl)cyclopropane-1,1-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77094-95-2

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77094-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77094-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,9 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77094-95:
(7*7)+(6*7)+(5*0)+(4*9)+(3*4)+(2*9)+(1*5)=162
162 % 10 = 2
So 77094-95-2 is a valid CAS Registry Number.

77094-95-2Relevant academic research and scientific papers

Lewis Acid-Catalyzed [3+3] Annulation of Donor-Acceptor Cyclopropanes and Indonyl Alcohols: One Step Synthesis of Substituted Carbazoles with Promising Photophysical Properties

Varshnaya, Rohit Kumar,Banerjee, Prabal

, p. 1614 - 1623 (2019/02/07)

A highly efficient protocol to access carbazole from donor-acceptor cyclopropane and indonyl alcohol via [3+3] annulation in the presence of a Lewis acid has been demonstrated. This method facilitates the post functionalization of the substituted carbazol

[3+3] Annulation via Ring Opening/Cyclization of Donor–Acceptor Cyclopropanes with (Un)symmetrical Ureas: A Quick Access to Highly Functionalized Tetrahydropyrimidinones

Taily, Irshad Maajid,Saha, Debarshi,Banerjee, Prabal

, p. 7804 - 7813 (2019/12/27)

A mild and straight-forward access to pharmacologically privileged tetrahydropyrimidinones exploiting readily available Donor–Acceptor cyclopropanes (DACs) is reported. This methodology involves the Lewis acid catalyzed synthesis of uriedo-malonates from (un)symmetrical ureas and DACs followed by I2-base mediated cyclization to their corresponding tetrahydropyrimidinones. The cyclization protocol involves nucleophilic attack of the nitrogen of urea on the newly generated electrophilic acceptor end of DAC. The post functionalization offered potential biologically active molecules.

Synthesis of Indenopyridine Derivatives via MgI2-Promoted [2+4] Cycloaddition Reaction of In-situ Generated 2-Styrylmalonate from Donor-Acceptor Cyclopropanes and Chalconimines

Verma, Kamal,Banerjee, Prabal

supporting information, p. 3687 - 3692 (2018/10/15)

An unexpected MgI2-promoted [2+4] cycloaddition reaction of in-situ generated 2-styrylmalonate from donor-acceptor cyclopropanes with chalconimines to synthesize highly substituted indenopyridine derivatives under the mild reaction conditions h

Cyclodimerization of 2-arylcyclopropane-1,1-diesters. Lewis acid induced reversion of cyclopropane umpolung

Chagarovskiy, Alexey O.,Ivanova, Olga A.,Budynina, Ekaterina M.,Trushkov, Igor V.,Melnikov, Mikhail Ya.

supporting information; experimental part, p. 4421 - 4425 (2011/09/19)

A novel Lewis acid catalyzed [3+2] cyclodimerization of 2-arylcyclopropane-1,1-dicarboxylates is reported. It is the first example of a reaction wherein a donor-acceptor cyclopropane provides two carbons in a newly formed ring. The described cyclodimeriza

(3 + 3)-cyclodimerization of donor-acceptor cyclopropanes. three routes to six-membered rings

Ivanova, Olga A.,Budynina, Ekaterina M.,Chagarovskiy, Alexey O.,Trushkov, Igor V.,Melnikov, Mikhail Ya.

experimental part, p. 8852 - 8868 (2012/01/02)

The ability of donor-acceptor cyclopropanes to (3 + 3)-cyclodimerize is disclosed. It has been found that Lewis acid-induced transformations of 2-(hetero)arylcyclopropane-1,1-dicarboxylates containing electron-abundant aromatic substituents led to the con

Lewis acid-catalyzed isomerization of 2-arylcyclopropane-1,1- dicarboxylates: A new efficient route to 2-styrylmalonates

Chagarovskiy, Alexey O.,Ivanova, Olga A.,Rakhmankulov, Eduard R.,Budynina, Ekaterina M.,Trushkov, Igor V.,Melnikov, Mikhail Ya.

supporting information; experimental part, p. 3179 - 3184 (2011/02/22)

A facile efficient approach to the 2-styrylmalonates via the Lewis acid-catalyzed isomerization of 2-arylcyclopropane-1,1-dicarboxylates has been developed. The efficiency of this method was demonstrated for a representative series of such cyclopropanes.

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