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(E)-2-Benzylidene-3-(cyclohexylamino)-2,3-dihydro-1H-inden-1-one is an indenone derivative with a molecular formula of C24H23NO. It features a benzylidene group and a cyclohexylamino group attached to the indenone ring, giving it a unique structure that holds potential in organic synthesis and medicinal chemistry.

1245792-51-1

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1245792-51-1 Usage

Uses

Used in Organic Synthesis:
(E)-2-Benzylidene-3-(cyclohexylamino)-2,3-dihydro-1H-inden-1-one is used as a building block for the synthesis of various organic compounds due to its distinctive chemical structure.
Used in Medicinal Chemistry:
(E)-2-Benzylidene-3-(cyclohexylamino)-2,3-dihydro-1H-inden-1-one is used as a potential candidate for biological activity exploration in medicinal chemistry, with the aim of discovering new therapeutic agents.
Further research and investigation into the properties and potential applications of (E)-2-Benzylidene-3-(cyclohexylamino)-2,3-dihydro-1H-inden-1-one are necessary to fully understand its capabilities and maximize its utility in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1245792-51-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,7,9 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1245792-51:
(9*1)+(8*2)+(7*4)+(6*5)+(5*7)+(4*9)+(3*2)+(2*5)+(1*1)=171
171 % 10 = 1
So 1245792-51-1 is a valid CAS Registry Number.

1245792-51-1Downstream Products

1245792-51-1Relevant articles and documents

In vivo structure-activity relationship studies support allosteric targeting of a dual specificity phosphatase

Korotchenko, Vasiliy N.,Saydmohammed, Manush,Vollmer, Laura L.,Bakan, Ahmet,Sheetz, Kyle,Debiec, Karl T.,Greene, Kristina A.,Agliori, Christine S.,Bahar, Ivet,Day, Billy W.,Vogt, Andreas,Tsang, Michael

, p. 1436 - 1445 (2014/07/21)

Dual specificity phosphatase 6 (DUSP6) functions as a feedback attenuator of fibroblast growth factor signaling during development. In vitro high throughput chemical screening attempts to discover DUSP6 inhibitors have yielded limited success. However, in

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