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1-(4-cyanophenyl)-N-(4-methoxyphenyl)methanesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1039967-79-7

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1039967-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1039967-79-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,9,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1039967-79:
(9*1)+(8*0)+(7*3)+(6*9)+(5*9)+(4*6)+(3*7)+(2*7)+(1*9)=197
197 % 10 = 7
So 1039967-79-7 is a valid CAS Registry Number.

1039967-79-7Relevant academic research and scientific papers

Straightforward Route to γ-Sultams via Novel Tandem S N/Michael Addition

Klochkova, Anastasiia,Bubyrev, Andrey,Dar'In, Dmitry,Bakulina, Olga,Krasavin, Mikhail,Sokolov, Viktor

, p. 1795 - 1804 (2021/02/09)

A novel tandem approach to trisubstituted γ-sultams has been developed involving N -alkylation of methanesulfonanilides with EWG-substituted allyl bromides followed by intramolecular Michael addition. A series of various isothiazolidine 1,1-dioxides have been prepared under mild transition-metal-free conditions in high yields and trans -diastereoselectivity (confirmed by X-ray crystallography). The dependence of reactivity on electronic properties of substrates has been investigated.

Access to a wide range of sultams by cyclodialkylation of α-substituted methanesulfonanilides

Rassadin, Valentin A.,Grosheva, Daria S.,Arefeva, Irina A.,Tomashevskiy, Aleksandr A.,Sokolov, Victor V.,De Meijere, Armin

supporting information, p. 5028 - 5037,10 (2020/08/24)

A wide range of five- and six-membered sultams bearing an α-ethoxycarbonyl-α-methyl substituent or an α-aryl group (17 examples) were synthesized by the cyclodialkylation of α-substituted methanesulfonanilides with α,ω-dihaloalkanes in the presence of K2CO3 or under phase-transfer catalysis (PTC) conditions. Upon treatment with K2CO3 in N,N-dimethylformamide (DMF) or NaH in dimethyl sulfoxide (DMSO), N-(2,3-dibromopropyl)-α- toluenesulfonanilides furnished different 1,3-diaryl-2-thia-3-azabicyclo[3.1.0] hexane 2,2-dioxides in good to excellent yields (51-88 %, 16 examples). The 4-methoxyphenyl (PMP) group was easily removed from the sultam nitrogen atom by treatment of the corresponding bicyclic sultams with cerium(IV) ammonium nitrate in acetonitrile (71-84 % yield, 6 examples). The intermolecular cyclodialkylation of α-substituted methanesulfonamides constitutes a simple and efficient route to five- and six-membered sultams with α-ethoxycarbonyl-α-methyl or α-aryl substitution. The intramolecular cyclodialkylation of N-(2,3-dibromopropyl)-α- toluenesulfanilides readily leads to bicyclic sultams bearing a cyclopropane ring. Copyright

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