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1352957-59-5

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  • 3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(8α,9S)-10,11-dihydro-6"-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione

    Cas No: 1352957-59-5

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  • 3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(8α;,9S)-10,11-dihydro-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione, 98%, (99% ee)

    Cas No: 1352957-59-5

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  • 3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(8α,9S)-10,11-dihydro-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione

    Cas No: 1352957-59-5

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1352957-59-5 Usage

General Description

The chemical "3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(8α,9S)-10,11-dihydro-6'-Methoxycinchonan-9-yl]aMino]-3-Cyclobutene-1,2-dione" is a complex compound with a cyclobutene-1,2-dione backbone and amino groups linked to a trifluoromethylphenyl and a cinchonan moiety. The trifluoromethylphenyl group is known for its electron-withdrawing properties, while the cinchonan moiety has potential biological activity. This chemical may have application in medicinal or pharmaceutical research due to its unique structure and potential binding properties. However, further research is necessary to determine its specific properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1352957-59-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,9,5 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1352957-59:
(9*1)+(8*3)+(7*5)+(6*2)+(5*9)+(4*5)+(3*7)+(2*5)+(1*9)=185
185 % 10 = 5
So 1352957-59-5 is a valid CAS Registry Number.

1352957-59-5Downstream Products

1352957-59-5Relevant articles and documents

Organocatalytic Enantioselective Michael-Addition of Malonic Acid Half-Thioesters to β-Nitroolefins: From Mimicry of Polyketide Synthases to Scalable Synthesis of γ-Amino Acids

Bae, Han Yong,Some, Surajit,Lee, Jae Heon,Kim, Ju-Young,Song, Myoung Jong,Lee, Sungyul,Zhang, Yong Jian,Song, Choong Eui

, p. 3196 - 3202 (2012/02/01)

Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs) to a variety of nitroolefins, affording the optically active γ-amino acid precursors, were developed by employing the Cinchona-based squaramides (up to >

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