180912-56-5

Usage

Structure

A cyclohexadiene ring with two carbonyl groups (C=O) at the 1 and 4 positions, a cyclohexylmethyl group at the 2 position, and a methoxy group (OCH3) at the 3 position.

Derivative of cyclohexadiene-1,4-dione

A common building block in organic chemistry.

Unique properties and potential applications

The addition of a cyclohexylmethyl group and a methoxy group to the molecule provide unique properties and potential applications in pharmaceuticals, agrochemicals, and materials science.

Valuable target for synthetic chemists

The compound's structure and functional groups make it a valuable target for synthetic chemists.

Contribution to the development of new drugs and materials

The compound's structure and functional groups could contribute to the development of new drugs and materials.

Upstream product

• 180912-52-1 2-Cyclohexylmethyl-1-methoxy-3-methoxymethoxy-benzene 
• 180912-50-9 Cyclohexyl-(2-methoxy-6-methoxymethoxy-phenyl)-methanol 
• 2550-36-9 Cyclohexylmethyl bromide 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 2043-61-0 cyclohexanecarbaldehyde 
• 57234-28-3 1-methoxy-3-(methoxymethoxy)benzene 
• 180912-54-3 2-Cyclohexylmethyl-3-methoxy-phenol 

Downstream Products

• 180912-59-8 2,3-Dichloro-5-cyclohexylmethyl-6-methoxy-[1,4]benzoquinone 
• 180912-65-6 2,6-Bis-cyclohexylmethyl-3,7-dihydroxy-8-methoxy-dibenzofuran-1,4-dione 
• 180912-63-4 2,6-bis(cyclohexylmethyl)-3,7,8-trimethoxydibenzofuran-1,4-dione 
• 180912-61-2 2-Chloro-5-cyclohexylmethyl-3-(3-cyclohexylmethyl-2-hydroxy-4,5-dimethoxy-phenyl)-6-methoxy-[1,4]benzoquinone 

Relevant academic research and scientific papers

Exploring the antimalarial potential of the methoxy-thiazinoquinone scaffold: Identification of a new lead candidate

A small library of antiplasmodial methoxy-thiazinoquinones, rationally designed on the model of the previously identified hit 1, has been prepared by a simple and inexpensive procedure. The synthetic derivatives have been subjected to in vitro pharmacolog

Synthesis of various model compounds for the central tricyclic ring system of popolophuanone E

An efficient synthesis of various model compounds 4a-e for the tricyclic core of popolophuanone E (1), a novel marine natural product, was accomplished; the method features highly regioselective annulation of the phenols 5a-e with the 2,3-dichloro-1,4-benzoquinones 7, 7c-e. Preliminary studies definitely demonstrated the feasibility of our designed synthetic strategy for 1 (the phenolic subunit I + the quinone subunit II → 1).