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2-(2-Nitro-vinyl)-benzo[b]thiophene is an organic compound characterized by its molecular formula C12H7NO2S. 2-(2-nitro-vinyl)-benzo[b]thiophene features a benzo[b]thiophene core, which is a fused ring system consisting of a benzene ring and a thiophene ring. The molecule is further distinguished by a vinyl group (C2H3) attached to the 2-position of the benzo[b]thiophene, and a nitro group (NO2) at the 2-position of the vinyl group. The nitro group introduces a strong electron-withdrawing effect, which can significantly influence the compound's reactivity and physical properties. This chemical structure may be relevant in various applications, such as in the synthesis of dyes, pharmaceuticals, or materials science, where its electronic properties and potential for further functionalization are of interest.

4565-36-0

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4565-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4565-36-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4565-36:
(6*4)+(5*5)+(4*6)+(3*5)+(2*3)+(1*6)=100
100 % 10 = 0
So 4565-36-0 is a valid CAS Registry Number.

4565-36-0Relevant academic research and scientific papers

Br?nsted Acid Catalyzed Dearomatization by Intramolecular Hydroalkoxylation/Claisen Rearrangement: Diastereo- and Enantioselective Synthesis of Spirolactams

Chen, Peng-Fei,Wang, Binju,Wu, Peng,Ye, Long-Wu,Zhou, Bo

supporting information, p. 27164 - 27170 (2021/11/22)

Described herein is a novel Br?nsted acid catalyzed intramolecular hydroalkoxylation/Claisen rearrangement, allowing the practical and atom-economic synthesis of a range of valuable spirolactams from readily available ynamides in generally good to excellent yields with excellent diastereoselectivities and broad substrate scope. Importantly, an unexpected dearomatization of nonactivated arenes and heteroaromatic compounds is involved in this tandem sequence. Moreover, an asymmetric version of this tandem cyclization was also achieved by efficient kinetic resolution by chiral phosphoric acid catalysis. In addition, the [3,3]-rearrangement is shown to be kinetically preferred over the related [1,3]-rearrangement by theoretical calculations.

17a-HYDROXYLASE/C17,20-LYASE INHIBITORS

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Paragraph 0275; 0276, (2014/03/21)

The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, R6, A and n are as defined herein. A deuteriated derivative of the compound of Formula (I) is also provided.

17α-HYDROXYLASE/C17,20-LYASE INHIBITORS

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Page/Page column 49, (2012/04/04)

The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, R6, A and n are as defined herein. A deuteriated derivative of the compound of Formula (I) is also provided.

Diversity-oriented synthesis of polycyclic diazinic scaffolds

Gigant, Nicolas,Claveau, Elise,Bouyssou, Pascal,Gillaizeau, Isabelle

, p. 844 - 847 (2012/03/26)

An efficient and versatile synthesis of a polycyclic diazinic system starting from oxazine has been developed using a two-step Michael/retro Michael and cyclization sequence. The substrates were synthesized with good to high yields giving rapid access to molecular diversity.

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