56136-14-2

Usage

Category

Synthetic Compound It is a man-made chemical that is not found naturally in the environment.

Applications

Dyes, Pigments, and Pharmaceuticals This substance is used in the production of various products, including dyes, pigments, and pharmaceuticals, due to its ability to undergo different chemical reactions.

Chemical Structure

Tetrahydroanthraquinone It is a derivative of anthraquinone, a type of organic compound that has a fused ring structure consisting of four carbon atoms and two oxygen atoms.

Industrial Processes

Commonly used The substance is widely utilized in various industrial processes due to its versatility and importance in the manufacturing of different products.

Versatility

Ability to undergo various chemical reactions This property makes it a valuable component in the production of a wide range of products, as it can be easily modified or combined with other substances to achieve desired outcomes.

InChI:InChI=1/C14H12O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-6,11-12H,7-8H2

Upstream product

• 64-17-5 ethanol 
• 106-99-0 buta-1,3-diene 
• 130-15-4 [1,4]naphthoquinone 
• 123-31-9 hydroquinone 

Downstream Products

• 90-44-8 anthracen-9(10H)-one 
• 84-65-1 9,10-phenanthrenequinone 
• 5520-99-0 2-benzenesulfonyl-anthraquinone 
• 1415995-30-0 2-benzenesulfonyl-9,10-dibutoxy-1,2-dihydroanthracene 
• 161363-52-6 1,4-dibenzyloxy-2,3-naphthalenediacetic acid 
• 161363-45-7 9,10-dibenzyloxy-1,4-dihydroanthracene-2,3-oxide 
• 161363-50-4 1,4-dibenzyloxy-2,3-naphthalenediacetaldehyde 
• 885-19-8 1,4-dihydro-9,10-anthraquinone 
• 161363-44-6 9,10-dibenzyloxy-1,4-dihydroanthracene 

Relevant academic research and scientific papers

A new 10-substituted -1, 4-dihydro-9-(meth) acrylate compound MS41-and its manufacturing method

PROBLEM TO BE SOLVED: To provide a compound having a high refractive index and causing no problem of absorption in the ultraviolet range or fluorescence. SOLUTION: The 1,4-dihydroanthracen-9-yl-(meth)acrylate compound is represented by formula (1). In the formula: Z1is an acryloyl group or a methacryloyl group; Z2is a hydrogen atom, an alkyl group, or an acyl group; and each of X and Y is any one of a hydrogen atom, an alkyl group and a halogen atom. COPYRIGHT: (C)2013,JPOandINPIT

Tetraaryltetraanthra[2,3]porphyrins: Synthesis, structure, and optical properties

A synthetic route to symmetrical tetraaryltetraanthra[2,3]porphyrins (Ar4TAPs) was developed. Ar4TAPs bearing various substituents in meso-phenyls and anthracene residues were prepared from the corresponding pyrrolic precursors. The synthesized porphyrins possess high solubility and exhibit remarkably strong absorption bands in the near-infrared region (790-950 nm). The scope of the method, selection of the peripheral substituents, choice of the metal, and their influence on the optical properties are discussed together with the first X-ray crystallographic data for anthraporphyrin.

New catalytic reactions in the presence of Mo-V-phosphoric heteropoly acid solutions

The possibility of performing new catalytic reactions in the presence of solutions of H x+3PMo12-x . VxO40 Mo-V-phosphoric heteropoly acids was examined.