Category: 578-95-0

Archives for Chemistry Experiments of 578-95-0

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578-95-0, Name is Acridin-9(10H)-one, molecular formula is C13H9NO, belongs to pyrrolines compound, is a common compound. In a patnet, author is Lu, Yi, once mentioned the new application about 578-95-0, Product Details of 578-95-0.

A new process for the synthesis of nafoxidene as a key intermediate of lasofoxifene

A novel brief process for the synthesis of nafoxidene has been developed. The epoxidation of 6-methoxy-1-{4-[2-(pyrrolin-1-yl)ethoxy)]phenyl}-3,4-dihydronaphthalene by m-CPBA directly gave the ketone 6-methoxy-1-[4-(2-(pyrrolidin-1-yl)ethoxy) phenyl]-3,4-dihydronaphthalen-2(1H)-one, which was subject to phenyl magnesium bromide/cerium chloride and subsequently treated with an acid to yield nafoxidene. In addition, the preparation of the starting naphthalene was also optimized by replacing the aromatic lithium at low temperature with its Grignard reagent at refluxing THF. This mild process, without the use of toxic or noble metals, was more cost-efficient and easily worked up.

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Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem

Extracurricular laboratory: Discover of Acridin-9(10H)-one

If you¡¯re interested in learning more about 578-95-0. The above is the message from the blog manager. Recommanded Product: Acridin-9(10H)-one.

578-95-0, Name is Acridin-9(10H)-one, molecular formula is C13H9NO, belongs to pyrrolines compound, is a common compound. In a patnet, author is Dairi, K, once mentioned the new application about 578-95-0, Recommanded Product: Acridin-9(10H)-one.

Two-step synthesis of the bipyrrole precursor of prodigiosins

The key intermediate in the synthesis of prodigiosins, 4-methoxy-2,2′-bipyrrole-5-carboxaldehyde, has been prepared in two steps and 65% overall yield from the commercially available 4-methoxy-3-pyrrolin-2-one. (c) 2006 Elsevier Ltd. All rights reserved.

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Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem

Extended knowledge of 578-95-0

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 578-95-0, you can contact me at any time and look forward to more communication. Recommanded Product: 578-95-0.

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. Recommanded Product: 578-95-0, 578-95-0, Name is Acridin-9(10H)-one, SMILES is C1=C2C(=CC=C1)C(C3=C(N2)C=CC=C3)=O, in an article , author is Grison, C, once mentioned of 578-95-0.

Enantioselective synthesis of alpha,beta-unsaturated gamma- and delta-lactams

An enantioselective synthesis of alpha,beta -unsaturated gamma- and delta -lactams was proposed based on a simple strategy using the initial preparation of c is vinylogous aminoesters by the Horner reaction followed by a mild intramolecular cyclisation. (C) 2001 Elsevier Science Ltd. All rights reserved.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 578-95-0, you can contact me at any time and look forward to more communication. Recommanded Product: 578-95-0.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem

More research is needed about Acridin-9(10H)-one

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 578-95-0 is helpful to your research. SDS of cas: 578-95-0.

Chemistry, like all the natural sciences, begins with the direct observation of nature¡ª in this case, of matter.578-95-0, Name is Acridin-9(10H)-one, SMILES is C1=C2C(=CC=C1)C(C3=C(N2)C=CC=C3)=O, belongs to pyrrolines compound. In a document, author is Pal, M, introduce the new discover, SDS of cas: 578-95-0.

A rapid and direct access to symmetrical/unsymmetrical 3,4-diarylmaleimides and pyrrolin-2-ones

1.8-Diazabicyclo[5.4.0]undec-7ene (DBU) facilitated the oxidative cyclization of phenacyl amide in the presence of atmospheric oxygen under environmentally friendly conditions. The reaction has been studied under various conditions and a plausible mechanism is proposed. This ‘green’ reaction proceeds via intramolecular ring closure of the amide followed by subsequent reaction with molecular oxygen where DBU played a crucial role. A variety of phenacyl amides were treated with DBU in acetonitrile under an oxygen atmosphere to dive the symmetrical/unsymmetrical 3.4-diarylsubstituted maleimides in good yields. Corresponding pyrrolin-2-ones however, were obtained in good to excellent yields when K2CO3 was used in place of DBU affording a practical synthesis of these compounds of potential biological interest. (C) 2004 Elsevier Ltd. All rights reserved.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 578-95-0 is helpful to your research. SDS of cas: 578-95-0.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem