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1′,3′-dioxo-3-phenyl-1′,3′-dihydrospiro[cyclopropane-1,2′-indene]-2,2-dicarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1334848-95-1

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1334848-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1334848-95-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,8,4 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1334848-95:
(9*1)+(8*3)+(7*3)+(6*4)+(5*8)+(4*4)+(3*8)+(2*9)+(1*5)=181
181 % 10 = 1
So 1334848-95-1 is a valid CAS Registry Number.

1334848-95-1Downstream Products

1334848-95-1Relevant academic research and scientific papers

Synthesis of Activated Cyclopropanes by MHIRC Strategy: A Facile and Efficient Approach to Spirocyclopropanes Using N-Halosulfon-amides

Ghorbani-Vaghei, Ramin,Maghbooli, Yaser

, p. 3803 - 3811 (2016)

In this study, a one-pot, three-component reaction of two molecules of indane-1,3-dione with aromatic aldehydes for the synthesis of spirocyclopropylindanediones using poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) (PBBS), N,N,N',N'-tetrabromobenzene-1,3-

Facile synthesis of spirosubstituted cyclopropanes through reaction of electron-deficient olefins and 1,3-indandione

Huang, Jiamin,Liu, Wenli,Wang, Changqing,Yang, Liu,Cao, Xiaohua

, (2020)

An efficient and facile approach for the synthesis of spirosubstituted cyclopropane derivatives has been described. The reaction of 1,3-indandione with arylidenemalononitrile in the presence of molecular iodine and dimethylaminopyridine occurred to give c

Synthesis of activated cyclopropanes by an MIRC strategy: An enantioselective organocatalytic approach to spirocyclopropanes

Russo, Alessio,Meninno, Sara,Tedesco, Consiglia,Lattanzi, Alessandra

scheme or table, p. 5096 - 5103 (2011/10/12)

An efficient cyclopropanation, by a Michael-initiated ring-closing (MIRC) reaction of 2-arylidene-1,3-indandiones and 2-arylidene malononitriles, has been developed by using different α-monohalogenated methylene active compounds with triethylamine. The first enantioselective cyclopropanation to spirocyclopropanes derived by the reaction of 2-arylidene-1,3-indandiones and dimethyl bromomalonate with a commercially available α,α-L- diarylprolinol as the organocatalyst and K2CO3 as the additive has been accomplished. The spirocyclopropanes were isolated in high yield and up to 85% ee. Notably, the asymmetric one-pot sequential approach to spirocyclopropanes proved to be a feasible process. A simple triethylamine-promoted domino cyclopropanation of 2-arylidene-1,3-indandiones and 2-arylidenemalononitriles with α-monohalogenated methylene-active compounds has been efficiently developed. Spirocyclopropanes derived from 2-arylidene-1,3-indandiones were synthesized with up to 85% ee by using dimethyl bromomalonate and α,α-L-diarylprolinol/K2CO3 system. Copyright

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