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1429048-37-2

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1429048-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429048-37-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,0,4 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1429048-37:
(9*1)+(8*4)+(7*2)+(6*9)+(5*0)+(4*4)+(3*8)+(2*3)+(1*7)=162
162 % 10 = 2
So 1429048-37-2 is a valid CAS Registry Number.

1429048-37-2Downstream Products

1429048-37-2Relevant academic research and scientific papers

Synthesis and anticancer activity of benzoselenophene and heteroaromatic derivatives of 1,2,9,9a-tetrahydrocyclopropa[c]benzo[e]indol-4-one (CBI)

Mhetre, Amol B.,Lee, Hangeun,Yang, Heekyoung,Lee, Kyoungmin,Nam, Do-Hyun,Lim, Dongyeol

, p. 1198 - 1208 (2017)

The current study reports the synthesis of different derivatives of benzoselenophene analogs as well as a diverse series of compounds (14a-p, 15 and 16) from 1,2,9,9a-tetrahydrocyclopropa[c]benzo[e]indol-4-one (CBI) and benzoselenophene or heteroaromatic acids. The overall yield of scaffold 12 was improved by an one-pot reaction, which helps in large-scale synthesis of CBI, a duocarmycin alkylation subunit analog. The series of compounds were evaluated for their cytotoxicity against SK-OV3 ovarian cancer cell lines, which revealed that benzoselenophene can enhance or maintain the anticancer activity of the duocarmycin analog upon replacing the indole moiety. CBI-benzoselenophenes with N-amido substituents at the C-5 position, 14g, 14f and 16 (IC50 = 0.5, 1.2 and 1.6 nM, respectively), were found to be more potent than the CBI-TMI and other benzoselenophene analogs. The CBI-benzoselenophene analogs, 14f and 14g (containing N-acetamido and N-butyramido substituents, respectively), were found to be 8 and 120 times more potent than the corresponding indole analogs of CBI, 14q and 14r, respectively.

SELENOPHENE-FUSED AROMATIC COMPOUND AND MANUFACTURING METHOD THEREOF

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Paragraph 0299, (2014/08/07)

The present disclosure relates to a method for more easily and economically producing a selenophene-fused aromatic compound derivative containing various substituents and the selenophene-fused aromatic compound produced according to the method, and the selenophene-fused aromatic compound can be used for various purposes such as an intermediate of an anti-bacterial or anticancer substance, an indicator of which color is changed depending on a solvent, or a fluorescent substance.

SELENOPHENE-FUSED AROMATIC COMPOUND AND MANUFACTURING METHOD THEREOF

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Paragraph 0101-0102, (2014/08/19)

The present disclosure relates to a method for more easily and economically producing a selenophene-fused aromatic compound derivative containing various substituents and the selenophene-fused aromatic compound produced according to the method, and the selenophenefused aromatic compound can be used for various purposes such as an intermediate of an anti-bacterial or anticancer substance, an indicator of which color is changed depending on a solvent, or a fluorescent substance.

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