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123 results about "Dithiane" patented technology

A dithiane is a heterocyclic compound composed of a cyclohexane core structure wherein two methylene bridges (-CH₂- units) are replaced by sulfur centres. The three isomeric parent heterocycles are 1,2-dithiane, 1,3-dithiane and 1,4-dithiane.

Alkenyl compound having a negative delta epsilon value, liquid crystal composition, and liquid crystal display device

There are provided a liquid crystalline compound having a large negative Deltaepsilon, low viscosity, a large K33 / K11 value, a small Deltaepsilon / epsilonL and mutually excellent solubility even at extremely low temperature; a liquid crystal composition prepared from a liquid crystalline compound; and a liquid crystal display device fabricated from such a liquid crystal composition. The liquid crystalline compound of the present invention is a liquid crystalline compound represented by the following general formula (1): where, R<1 >represents hydrogen, fluorine, an alkyl group having 1 to 15 carbon atoms, or an alkenyl group having 2 to 15 carbon atoms; each of rings A<1>, A<2>, and A<3 >independently represents trans-1,4-cyclohexylene group, 1,4-cyclohexenylene group, trans-1,4-silacyclohexylene group, 1,4-phenylenegroup, 2,3-difluoro-1,4-phenylene group, 2-fluoro-1,4-phenylene group, 3-fluoro-1,4-phenylene group, pyrimidine-2,5-diyl group, pyridine-2,5-diyl group, 1,3-dioxane-2,5-diyl group, tetrahydropyrane-2,5-diyl group, 1,3-dithiane-2,5-diyl group, or tetrahydrothiopyrane-2,5-diyl group; X<1 >represents hydrogen or fluorine; Y<1 >represents hydrogen or an alkyl group having 1 to 15 carbon atoms; 1 represents an integer from 1 to 10; and each of m and n independently represents 0 or 1.
Owner:JNC CORP

Pure and stable tiotropium bromide

This invention relates to solvates of tiotropium bromide having a purity of at least 99%, process for preparing such pure solvates, and their use in pharmaceutical formulations. This invention also provides tiotropium bromide solvates containing less than about 0.15% area by HPLC of 2,2-dithienyl glycolic acid.
Owner:SICOR SOC ITAL CORTICOSTEROIDI SPA

Holographic recording medium

A holographic recording medium includes a recording layer. The recording layer includes a framework being expressed with the following general formula (1),In the above formula (1), Ar represents a substituted or unsubstituted group selected from benzothiophene group, naphthothiophene group, dibenzothiophene group, thienothiophene group, dithienobenzene group, benzothiazole group, naphthothiazole group, benzoisothiazole group, naphthoisothiazole group, phenothiazine group, phenoxathiin group, dithianaphthalene group, thianthrene group, thioxanthene group, and bithiophene group. In addition, n is an integer from 1 to 4.
Owner:KK TOSHIBA

Method for preparing tiotropium bromide

The invention discloses a method for preparing tiotropium bromide, which comprises the following steps of: preparing scopine-2,2-dithienyl glycolate from scopine and methyl 2,2-dithienyl glycolate, reacting the scopine-2,2-dithienyl glycolate with methyl bromide to prepare a tiotropium bromide crude product, and refining the tiotropium bromide crude product to obtain a tiotropium bromide finishedproduct. The method is characterized in that: the scopine and the methyl 2,2-dithienyl glycolate undergo ester exchange reaction under the action of dimethylbenzene, and the mixed catalysts of sodiumand sodium methoxide, and after the reaction, reaction solution is post-treated to obtain the scopine-2,2-dithienyl glycolate. In the method, in the process of preparing the scopine-2,2-dithienyl glycolate, the sodium and the sodium methoxide are simultaneously taken as the catalysts, and scopine isomer content after the reaction is less than 0.1 percent which completely meets specifications in the trial standards of European pharmacopoeia; and the method solves a big problem for the conventional preparation of the tiotropium bromide and is easy to realize industrial production.
Owner:ANHUI DEXINJIA BIOPHARM

Synthetic method of 1,3-dithiane structure-containing polysubstituted olefin derivatives

The invention relates to a synthetic method of 1,3-dithiane structure-containing polysubstituted olefin derivatives. The method comprises the following steps: carrying out an oxyradical coupling reaction on 1,3-dithiane and polysubstituted olefins in a solvent in the presence of a catalyst Lewis acid and an activator N-chlorosuccimide with air or oxygen as an oxidant, separating, and purifying to obtain the 1,3-dithiane structure-containing polysubstituted olefin derivatives. The method has the advantages of avoiding of use of a metal catalyst due to cheap and easily available substrates used in the invention, environmental protection, simple reaction process and mild conditions, the 1,3-dithiane structure-containing polysubstituted olefin derivatives have good function group tolerance and can be directly obtained through a one-kettle process, the method has beneficial technical effects, and can be well applied in scientific researches and industrial production.
Owner:LANZHOU UNIVERSITY

Photoacid generator and photoreactive composition

An object of the present invention is to provide photoacid generator, which shows very high sensitivity in the near ultraviolet range of about 300 to 400 nm, and also can remarkably increase a reaction rate of a photoreactive composition using the same, and to provide a photoreactive composition which can initiate the reaction even by irradiation with near ultraviolet light within a short time and also can obtain a desired reaction product. More particularly, the present invention provides a dithienyl sulfide disulfonium salt represented by the formula (A1):
wherein R1a to R4a each independently represents an optionally substituted monocyclic carbon ring group, an optionally substituted condensed polycyclic carbon ring group or an optionally substituted monocyclic heterocyclic group, and X represents an inorganic acid ion or an organic acid ion; a photoacid generator containing the dithienyl sulfide disulfonium salt, and a photoreactive composition containing the photoacid generator and an acid reactive compound; a dithienyl sulfide sulfonium salt represented by the formula (B1):
wherein R1b and R2b each independently represents an optionally substituted monocyclic carbon ring group, an optionally substituted condensed polycyclic carbon ring group or an optionally substituted monocyclic heterocyclic group, R3b to R5b each independently represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, an acyl group or a hydroxyl group, and X represents an inorganic acid ion or an organic acid ion, a photoacid generator containing the same, and a photoreactive composition containing the photoacid generator; and a phenylthiothiophene sulfonium salt represented by the formula (C1):
wherein R1c and R2c each independently represents an optionally substituted monocyclic carbon ring group, an optionally substituted condensed polycyclic carbon ring group or an optionally substituted monocyclic heterocyclic group, and R3c to R7c each independently represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, alkoxy group having 1 to 4 carbon atoms, an acyl group or a hydroxyl group, and X represents an inorganic acid ion or an organic acid ion, a photoacid generator containing the same, and a photoreactive composition containing the photoacid generator and an acid reactive compound.
Owner:SUMITOMO SEIKA CHEM CO LTD

Preparation method of anti-sulfur poisoning platinum complex

The invention provides a preparation method of an anti-sulfur poisoning platinum complex. The preparation method comprises the following steps: preparing a 1,3-dithiane benzene containing derivative intermediate A, preparing an unsaturated symmetrical epithio-silane intermediate B, connecting the 1,3-dithiane benzene containing derivative intermediate A to Pt through a phase transfer substitutionbond, then firstly substituting and then chelating the unsaturated symmetrical epithio-silane intermediate B to Pt, and obtaining the anti-sulfur poisoning platinum complex. The preparation method issimple and convenient, the reaction condition is mild, the production efficiency is high, the cost is low, and the industrial production is realized. A prepared catalyst has a highly symmetric complexstructure, the anti-sulfur poisoning platinum complex is stable at the room temperature, can be stored for long and has an excellent anti-sulfur poisoning catalytic effect, the catalytic activity ismore than 92%, the curing degrees of a sulfur-containing system and a non-sulfur system are basically the same and both reach more than 90%, and the anti-sulfur poisoning platinum complex has an excellent anti-sulfur poisoning capability, and is widely applied to the hydrosilylation.
Owner:GUANGDONG UNIV OF TECH

D-A-D type organic photo-thermal small molecular material and preparation method thereof

The invention provides a D-A-D type organic photo-thermal small molecular material and a preparation method thereof. The D-A-D type organic photo-thermal small molecular material contains an electronwithdrawing group 2,1,3-benzothiadiazole and an electron donating group 3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo[3,4-c] pyrrole-1,4-dione. The preparation method comprises the steps: substituting H ona thiophene ring of bromo-isooctane substituted 3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione with N-bromo-succinimide, and carrying out a reaction with 2,1,3-benzothiadiazole-4,7-bis(pinacol borate) through Suzuki reaction to obtain the target product. With the introduction of an alkyl chain on the side chain of the electron donating group, the solubility of the organic photo-thermal material in the organic solvent is improved, the problem of poor solubility of the organic polymer is overcome, and favorable light stability is achieved.
Owner:SHANXI UNIV
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