Category: 35212-85-2

35212-85-2, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In a patent, 35212-85-2, molecular formula is C10H9NO2S, introducing its new discovery.

Novel hetero-cyclic compound and organic light emitting device comprising the same

The present invention refers to novel heterocyclic compound and organic light emitting number including […] substrate. (by machine translation)

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.35212-85-2, you can also check out more blogs about35212-85-2

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Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

 

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬Which mentioned a new discovery about 35212-85-2, molcular formula is C10H9NO2S, introducing its new discovery. , 35212-85-2

CONDENSED COMPOUND AND ORGANIC LIGHT EMITTING DEVICE INCLUDING THE SAME

Disclosed is a novel condensed cyclic compound and an organic light emitting device including the same.COPYRIGHT KIPO 2015

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, 35212-85-2, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 35212-85-2

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Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

 

35212-85-2, In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 35212-85-2, name is Methyl 3-aminobenzo[b]thiophene-2-carboxylate, introducing its new discovery.

A red phosphorescent compound and its use the organic light-emitting device (by machine translation)

The invention relates to a red phosphorescent compounds and the use of the compounds of the organic light emitting device, more specifically, relates to a has excellent color purity and high brightness and light-emitting efficiency of the soluble phosphorescent compounds and the use of the compounds of the OLED device. A phosphorescent compounds, as shown in structural formula I, In the above formula I, Z is independently selected from the following structure: Wherein Ar independently selected from C6 – C30 aryl, C2 – C30 heteroaryl in a. The C6 – C30 aryl group selected from phenyl, naphthyl, biphenylyl, terphenylyl and phenanthrene-one. The C2 – C30 heteroaryl selected from pyridyl, linked pyridyl, quinolyl, isoquinolyl, phenanthroline-based and triazine-based one. This invention uses the I as shown in the chemical formula of the organic light emitting diode device of the luminescent layer, has excellent color purity and brightness and the effect of the extension of the durability. (by machine translation)

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.35212-85-2, you can also check out more blogs about35212-85-2

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Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

 

35212-85-2, Methyl 3-aminobenzo[b]thiophene-2-carboxylate is a benzothiophene compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A. 3-Aminobenzothiophene (20A) To a solution of 3-amino-benzo[b]thiophene-2-carboxylic acid, methyl ester (1 g, 4.83 mmol, 1 eq) in 1-methyl-2-pyrrolidinone (8 mL) was added piperazine (2.08 g, 24.13 mmol, 5 eq). The reaction was stirred at 130 C. overnight. Ice was added, and the mixture was extracted with ethyl acetate. The organic extracts were washed twice with water, dried, and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel eluding with 40% ethyl acetate in hexanes to provide 600 mg (83%) of Compound 20A as a yellow oil., 35212-85-2

The synthetic route of 35212-85-2 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Salvati, Mark E.; Balog, James Aaron; Shan, Weifang; Giese, Soren; US2003/114420; (2003); A1;; ; Patent; Salvati, Mark E.; Balog, James Aaron; Shan, Weifang; Giese, Soren; Harikrishnan, Lalgudi S.; US2004/77606; (2004); A1;,
Benzothiophene – Wikipedia
Benzothiophene | C8H6S – PubChem

 

35212-85-2, Methyl 3-aminobenzo[b]thiophene-2-carboxylate is a benzothiophene compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

Step 1 1-(Benzothiophen-3-yl)piperazine To a solution of methyl 3-aminobenzothiophene-2-carboxylate [prepared by the method of J. R. Beck, J. Org. Chem. 1972, 37, 3224] (6.5 g, 31.4 mmol) in N-methylpyrrolidinone (30 ml) was added 1-methylpiperazine and the reaction mixture was heated to 178 C. for 4 h. After cooling the mixture was poured into water and the product extracted with diethyl ether (3*100 ml), the extracts were washed with water (1*100 ml) and brine (1*100 ml), combined and dried (MgSO4). Concentration of the extracts yielded 3-aminobenzothiophene (5.9 g), which was used without purification., 35212-85-2

As the paragraph descriping shows that 35212-85-2 is playing an increasingly important role.

Reference£º
Patent; Merck Sharpe & Dohme Ltd.; US5432177; (1995); A;,
Benzothiophene – Wikipedia
Benzothiophene | C8H6S – PubChem