80171-39-7

Upstream product

• 619-23-8 3-Nitrobenzyl chloride 
• 64-17-5 ethanol 
• 141-52-6 sodium ethanolate 
• 3958-57-4 1-bromomethyl-3-nitrobenzene 
• 5188-07-8 sodium thiomethoxide 
• 619-25-0 3-Nitrobenzyl alcohol 

Downstream Products

• 618-98-4 ethyl 3-nitrobenzoate 
• 99-61-6 3-nitro-benzaldehyde 
• 111278-32-1 α-hydroperoxy-m-nitrobenzyl ethyl ether 
• 80171-96-6 3-(ethoxymethyl)aniline 

Relevant academic research and scientific papers

Liquid crystal aligning agent for photoalignment, liquid crystal alignment film and liquid crystal display device using it, and diamine and polymer

Provided are a liquid crystal alignment film capable of being given anisotropy through photoalignment and stable to light, and a liquid crystal display device capable of keeping a high voltage holding ratio without degradation of display quality even when

AZOBENZENE DERIVATIVE AND MANUFACTURING METHOD THEREFOR

PROBLEM TO BE SOLVED: To provide an azobenzene derivative useful as an intermediate of 2-substituted 4,4'-diaminoazobenzene used as a manufacturing raw material of a polyimide optical oriented film for liquid crystal display, and an effective manufacturing method therefor. SOLUTION: There is provided an azobenzene derivative represented by the general formula (1). R1 represents a hydrogen atom, an alkyl group which may be substituted, an acyl group which may be substituted and an alkoxycarbonyl group which may be substituted. R2 represents a hydrogen atom, an arylmethyl group which may be substituted, an alkali metal oxysulfonyl methyl group or an alkoxycarbonyl group which may be substituted. R3 is a nitro group, an arylmethylamino group which may be substituted, an alkali metal oxysulfonyl methylamino group, or an alkoxycarbonyl amino group which may be substituted. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

METHODS FOR INHIBITING NECROPTOSIS

The present invention relates to methods for inhibiting necroptosis; screening methods for identifying compounds which inhibit necroptosis; and compounds for the inhibition of necroptosis, which may be useful in the treatment of conditions associated with deregulated necroptosis.

CYCLOHEXANE DERIVATIVE COMPOUND

To find a therapeutic and/or prophylactic agent for gastrointestinal disorders and so on, the agent having excellent activity and high safety. A compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof. In the formula, A represents an optionally substituted phenylene group; B represents an optionally substituted 4- to 10-membered heterocyclic group, an optionally substituted C6-C10 aryl group, or an optionally substituted C3-C10 cycloalkyl group; R1 represents a hydrogen atom or a C1-C3 alkyl group; R2 represents a hydrogen atom or a C1-C3 alkyl group; R3 represents a C1-C6 alkyl group, a C3-C10 cycloalkyl group, a C1-C3 alkoxy C1-C3 alkyl group, or a C1-C3 hydroxyalkyl group; R4 represents a hydrogen atom, a C1-C6 alkyl group, or a halogen atom; n represents an integer of 1 to 4; and X represents methylene, -O-, -NH-, -N(C1-C3 alkyl)-, -C(=O)-, -S-, -S(O)-, -S(O2)- or a single bond.

Photooxygenation of nitrobenzyl derivatives. Mechanism of photogeneration and hydrolysis of α-hydroperoxy nitrobenzyl ethers

The photooxygenation of nitrobenzyl derivatives 1-10 has been studied in aqueous solution as a function of pH.For m-nitrobenzyl ethers 2-4 and 9, stable α-hydroperoxy ethers (11-13) are the primary photochemical products.Acid hydrolysis of 11-13 gives m-nitrobenzaldehyde and hydrogen peroxide.Quantum yields for photooxygenation are reported for a number of derivatives as a function of pH.Acid and base catalyses of photooxygenation are observed for several compounds.A mechanism involving photogenerated nitrobenzyl carbanion intermediates is proposed.

N-Alkyl-N-[3-(alkoxyalkyl)phenyl]-2-haloacetamide herbicides

This invention concerns certain N-alkyl-N-[3-(alkoxyalkyl)phenyl]-2-haloacetamides having herbicidal activity, their preparation, and the control of weeds therewith.