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2-(3,4-DIMETHOXY-PHENYL)-N-METHOXY-N-METHYL-ACETAMIDE is a chemical compound with the molecular formula C12H17NO4. It is a derivative of acetamide with a methoxy and methyl group attached to the nitrogen atom and a dimethoxy-phenyl group attached to the carbon atom.
Used in Scientific Research:
2-(3,4-DIMETHOXY-PHENYL)-N-METHOXY-N-METHYL-ACETAMIDE is used as a research tool for studying neurobiology and pharmacology due to its potential biological activities.
Used in Pharmaceutical Applications:
2-(3,4-DIMETHOXY-PHENYL)-N-METHOXY-N-METHYL-ACETAMIDE is used in the development of new drugs, as it exhibits potential biological activities that may contribute to therapeutic effects.
Used in Organic Synthesis:
2-(3,4-DIMETHOXY-PHENYL)-N-METHOXY-N-METHYL-ACETAMIDE is used as a chemical intermediate in the field of organic synthesis and chemical reactions, enabling the creation of various compounds with specific properties.

155955-78-5

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155955-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155955-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,5 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155955-78:
(8*1)+(7*5)+(6*5)+(5*9)+(4*5)+(3*5)+(2*7)+(1*8)=175
175 % 10 = 5
So 155955-78-5 is a valid CAS Registry Number.

155955-78-5Relevant articles and documents

Synthesis of Benzo[ b]furans by Intramolecular C-O Bond Formation Using Iron and Copper Catalysis

Henry, Martyn C.,Sutherland, Andrew

supporting information, p. 2766 - 2770 (2020/03/30)

One-pot processes for the synthesis of benzo[b]furans from 1-aryl- or 1-alkylketones using nonprecious transition metal catalysts have been developed. Regioselective iron(III)-catalyzed halogenation of the aryl ring, followed by iron- or copper-catalyzed O-arylation allowed the synthesis of various structural analogues, including the benzo[b]furan-derived natural products corsifuran C, moracin F, and caleprunin B.

Facile o-quinodimethane formation from benzocyclobutenes triggered by the Staudinger reaction at ambient temperature

Kohyama, Aki,Koresawa, Eri,Tsuge, Kiyoshi,Matsuya, Yuji

supporting information, p. 6205 - 6208 (2019/06/07)

Electron-donating iminophosphoranes were found to significantly enhance 4π-ring opening of benzocyclobutenes to generate o-quinodimethanes at 20-25 °C. These iminophosphorane benzocyclobutenes can be conveniently generated from azide benzocyclobutenes and phosphines via the Staudinger reaction. Thus, Staudinger reaction-triggered sequential molecular transformations of the azide benzocyclobutenes have been established via o-quinodimethanes at ambient temperature, which is expected to exhibit potential for a wide range of applications.

Novel dihydroquinolizinones for the treatment and prophylaxis of hepatitis B virus infection

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Paragraph 1315; 1316; 2045; 2046, (2015/08/04)

The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds.

NOVEL DIHYDROQUINOLIZINONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

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Page/Page column 175; 321; 322, (2015/09/23)

The invention provides novel compounds having the general formula (I) wherein R1, R2 R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds in the treatment of the hepatitis B virus.

NOVEL DIHYDROPYRIMIDIN-2(1H)-ONE COMPOUNDS AS S-NITROSOGLUTATHIONE REDUCTASE INHIBITORS

-

Page/Page column 138, (2011/04/24)

The present invention is directed to novel dihydropyrimidin-2(1H)-one compounds useful as S-nitrosoglutathione reductase (GSNOR) inhibitors, pharmaceutical compositions comprising such compounds, and methods of making and using the same.

Synthesis, structure-activity relationship, and receptor pharmacology of a new series of quinoline derivatives acting as selective, noncompetitive mGlu1 antagonists

Mabire, Dominique,Coupa, Sophie,Adelinet, Christophe,Poncelet, Alain,Simonnet, Yvan,Venet, Marc,Wouters, Ria,Lesage, Anne S. J.,Van Beijsterveldt, Ludy,Bischoff, Fran?ois

, p. 2134 - 2153 (2007/10/03)

We describe the discovery and the structure-activity relationship of a new series of quinoline derivatives acting as selective and highly potent noncompetitive mGlu1 antagonists. We first identified cis-10 as a fairly potent mGlu1 antagonist (IC50/s

5,6,7-Trisubstituted 4-Aminopyrido[2,3-d]pyrimidines as Novel Inhibitors of Adenosine Kinase

Perner, Richard J.,Gu, Yu-Gui,Lee, Chih-Hung,Bayburt, Erol K.,McKie, Jeffery,Alexander, Karen M.,Kohlhaas, Kathy L.,Wismer, Carol T.,Mikusa, Joe,Jarvis, Michael F.,Kowaluk, Elizabeth A.,Bhagwat, Shripad S.

, p. 5249 - 5257 (2007/10/03)

The synthesis and structure-activity relationship of a series of 5,6,7-trisubstituted 4-aminopyrido[2,3-d]pyrimidines as novel nonnucleoside adenosine kinase inhibitors is described. A variety of alkyl, aryl, and heteroaryl substituents were found to be tolerated at the C5, C6, and C7 positions of the pyridopyrimidine core. These studies have led to the identification of analogues that are potent inhibitors of adenosine kinase with in vivo analgesic activity.

5,6,7-trisubstituted-4-aminopyrido[2,3-D] pyrimidine compounds

-

, (2008/06/13)

A compound having the formula wherein R1, R2, R3, R4 and R5 are defined, a method for inhibiting adenosine kinase by administering a compound thereof, a pharmaceutical composition comprising a therapeutically effective amount of a compound thereof above i

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