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96 results about "9H-carbazole" patented technology

The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. 9H-Carbazole is included on this list.

A process for preparation of 1-[9h-carbazol-4-yloxy]-3-[{2-(2-(methoxy)phenoxy)-ethyl}-amino]-propan-2-ol

The present invention provides a process for preparation of 1-[9H-carbazol-4-yloxy]-3-[{2-(2-(methoxy)phenoxy)-ethyl}-amino]-propan-2-ol, a compound of formula 1 in racemic form or in the form of optically active R or S enantiomer or its pharmaceutically acceptable salt, comprising, reacting 4-(oxiranylmethoxy)-9H-carbazole, a compound of formula (2) or the R or S enantiomer thereof with a compound of formula (5), wherein R1 is benzyl or substituted benzyl group, in an aprotic organic solvent in presence of a catalyst to obtain a compound of formula (6), or the R or S enantiomer thereof, wherein R1 is as defined above. The resultant compound of formula (6) is subjected to debenzylation reaction by catalytic hydrogenation to obtain the compound of formula (1), if desired converting the resultant compound of formula (1) to a pharmaceutically acceptable salt thereof.
Owner:SUN PHARMA INDS

Phosphine-oxygen red/orange thermally activated delayed fluoresce material as well as synthesis method and application thereof

The invention discloses a phosphine-oxygen red / orange thermally activated delayed fluoresce material as well as a synthesis method and application thereof, relates to the thermally activated delayed fluoresce material as well as the synthesis method and the application thereof, and aims to solve the problems that a conventional red / orange TADF (Thermally Activated Delayed Fluoresce) material is slightly low in concentration quenching and electroluminescent device efficiency and rapid in attenuation because of high molecular polarity. The structural formula of the material is as shown in the specification. The synthesis method comprises the following steps: preparing 9-(2-bromine-4-(1,3-dioxolane-2-yl) phenyl-9H-carbazole or 9-(2-bromine-4-(1,3-dioxolane-2-yl) phenyl)-3,6-ditert-butyl-9H-carbazole, preparing 4-(9H-carbazole-9-yl)-3-(diphenylphosphine oxide) benzaldehyde or 4-(3,6-ditert-butyl-9H-carbazole-9-yl)-3-(diphenylphosphine oxide) benzaldehyde, and preparing a final product. By adopting the material disclosed by the invention, the efficiency of an electroluminescent device is remarkably improved, the quenching effect is reduced, and the efficiency stability of the electroluminescent device is improved. The material belongs to the field of fluorescence material preparation.
Owner:JIANGSU FUXIN ELECTRONICS LIGHTING TECH

Polycarboxylic acid carbazole ligand-based indium-organic skeleton material and preparation method thereof

The invention relates to a polycarboxylic acid carbazole ligand-based indium-organic skeleton material and a preparation method thereof, and belongs to the technical field of crystalline materials. The chemical molecular formula is [(CH3)2NH2][InL].5H2O, wherein L is organic ligand 4,4',4'',4'''-(9H-carbazole-1,3,6,8-tetrasubstituted) para-benzoic acid radical. Organic ligand 4,4',4'',4'''-(9H-carbazole-1,3,6,8-tetrasubstituted) para-benzoic acid and indium nitrate are dissolved into a solution of N,N'-dimethylacetamide and tetrafluoroboric acid, and solvent thermal reaction is conducted to obtain the metal organic skeleton material. The metal organic skeleton material has a dye adsorption property and can be applied to industrial dye treatment.
Owner:BEIJING UNIV OF TECH

Novel carbazole fluorescent thiol marking reagent as well as synthesis method and application thereof

The invention provides a novel carbazole fluorescent thiol marking reagent as well as a synthesis method and application thereof. The florescent marking reagent adopts carbazole as a fluorescent basering and activated C=C double bonds as reaction activity groups, is simple and convenient in synthesis step, easy to operate and can be synthesized in a large scale through two steps of reactions as follows: (1) enabling carbazole to react with 4-bromobenzaldehyde so as to obtain an intermediate (4-(9H-carbazole-9-yl) benzaldehyde; (2) enabling the intermediate (4-(9H-carbazole-9-yl) benzaldehydeto react with malononitrile so as to obtain a target product (4-(9H-carbazole-9-yl) benzaldehyde malononitrile, and performing recrystallization for three times with acetonitrile, thereby obtaining ayellow needle-shaped crystal. The chemical purity of the fluorescent marking reagent provided by the invention is up to 99%, and the fluorescent marking reagent is stable in chemical property. The novel carbazole fluorescent thiol marking reagent provided by the invention is capable of rapidly and accurately marking degradation thiol products of organic thiol ester insecticides under a gentle condition, and quantitative analysis on contents of organic thiol ester insecticides in reagent samples can be achieved.
Owner:QUFU NORMAL UNIV

Preparation method of phenylalanine compound

The invention discloses a preparation method of 2-(2-(4-fluorobenzoyl)phenylamino)-3-(4-(2-(9H-carbazole-9-yl)ethoxy)phenyl) propionic acid. The method comprises the step: carrying out condensation, hydrolysis and acidification on 9-carbazole ethyl alcohol methanesulfonate and 2-[(2-(4-fluorobenzoyl)phenyl)amino]-3-(4-hydroxyphenyl) methyl propionate serving as initial raw materials to obtain a target compound. The preparation method disclosed by the invention is suitable for industrial production, and the obtained target compound is high in purity.
Owner:SHENZHEN CHIPSCREEN BIOSCIENCES CO LTD
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