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3-(4-methylphenyl)cyclopropane-1,1,2,2-tetracarbonitrile is a complex organic compound characterized by its unique molecular structure. It features a cyclopropane ring, which is a three-carbon ring, with each carbon atom bonded to a nitrile group (-CN). Additionally, one of the carbons in the cyclopropane ring is connected to a 4-methylphenyl group, which is a phenyl ring (a six-carbon ring with alternating double bonds) with a methyl group (-CH3) attached to the fourth carbon. 3-(4-methylphenyl)cyclopropane-1,1,2,2-tetracarbonitrile is known for its rigid structure due to the cyclopropane ring and the presence of multiple nitrile groups, which can participate in various chemical reactions, such as addition and polymerization. It is typically synthesized for use in the production of specialty chemicals and materials, where its specific structural properties are leveraged for particular applications.

23767-71-7

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23767-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23767-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,6 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23767-71:
(7*2)+(6*3)+(5*7)+(4*6)+(3*7)+(2*7)+(1*1)=127
127 % 10 = 7
So 23767-71-7 is a valid CAS Registry Number.

23767-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methylphenyl)cyclopropane-1,1,2,2-tetracarbonitrile

1.2 Other means of identification

Product number -
Other names 3-(4-methylphenyl)-1,1,2,2-tetracyanocyclopropane

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:23767-71-7 SDS

23767-71-7Downstream Products

23767-71-7Relevant academic research and scientific papers

Synthesis of 3-Arylcyclopropane-1,1,2,2-tetracarbonitriles under Micellar Catalysis

Bardasov,Alekseeva, A. Yu.,Bezgin,Ershov

, p. 1839 - 1841 (2018)

An environmentally benign procedure has been developed for the synthesis of 3-arylcyclopropane- 1,1,2,2-tetracarbonitriles in an aqueous surfactant solution.

Pyridinium bromide as a new mediator for electrochemical transformations involving CH-acids

Vereshchagin, Anatoly N.,Dorofeeva, Evgeniya O.,Elinson, Michail N.,Korolev, Victor A.,Egorov, Mikhail P.

, p. 391 - 392 (2019/08/20)

Pyridinium bromide has been tested as a new mediator for electrochemical synthesis of functionalized cyclopropane from alkylidenemalononitriles and CH-acids. The process was performed in an undivided cell with the use of substoichiometric amount of PyHBr

Pyridinium bromide as a mediator in electrochemical reactions: The preparation of cyclopropane-1,1-dicarbonitriles

Vereshchagin, Anatoly N.,Dorofeeva, Evgeniya O.,Elinson, Michail N.,Egorov, Mikhail P.

, p. 325 - 335 (2020/02/13)

Pyridinium bromide has been tested as a new mediator for electrochemical transformations in methanol and acetonitrile. An efficient protocol for the synthesis of cyclopropanes via the electrochemical transformations of alkylidenemalononitriles and C-H aci

A new type of cascade reaction: direct conversion of carbonyl compounds and malononitrile into substituted tetracyanocyclopropanes

Elinson, Michail N.,Vereshchagin, Anatolii N.,Stepanov, Nikita O.,Ilovaisky, Alexey I.,Vorontsov, Alexander Ya.,Nikishin, Gennady I.

experimental part, p. 6057 - 6062 (2011/03/19)

A new type of chemical cascade reaction was found: the direct formation of cyclopropanes from carbonyl compounds and C-H acid. The action of free halogen or active halogen containing compounds on a mixture of 1 equiv of carbonyl compound and 2 equiv of malononitrile in a basic alcohol solution results in the formation of substituted 1,1,2,2-tetracyanocyclopropanes in 15-80% yield. The latter are well-known precursors for the different bicyclic heterosystems, among them compounds containing a cyclopropane ring and possessing different types of pharmacological activity. Thus, the new, simple and efficient 'one-pot' way to substituted tetracyanocyclopropanes in 50-80% yield was found directly from such simple and reasonable starting compounds as aldehydes, or some cyclic ketones, or substituted cyclohexanones and malononitrile.

One-pot cascade assembling of 3-substituted tetracyanocyclopropanes from alkylidenemalononitriles and malononitrile by the only bromine direct action

Vereshchagin, Anatolii N.,Elinson, Michail N.,Stepanov, Nikita O.,Nikishin, Gennady I.

experimental part, p. 324 - 325 (2010/01/18)

The new cascade reaction was found: the formation of cyclopropanes from alkylidenemalononitriles and malononitrile by the only bromine direct action; the action of aqueous bromine on the equal amounts of alkylidenemalononitriles and malononitrile in EtOH-

A new strategy of the chemical route to the cyclopropane structure: direct transformation of benzylidenemalononitriles and malononitrile into 1,1,2,2-tetracyanocyclopropanes

Elinson, Michail N.,Feducovich, Sergey K.,Stepanov, Nikita O.,Vereshchagin, Anatolii N.,Nikishin, Gennady I.

, p. 708 - 713 (2008/09/16)

The new reaction was found: the direct formation of cyclopropanes from activated olefins and C-H acids. The action of free halogen or active halogen containing compounds on the equal amounts of benzylidenemalononitriles and malononitrile in basic alcohol

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