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6-methoxy-1-methyl-2-phenyl-4(1H)-quinolinone is a complex organic compound belonging to the quinolinone family, characterized by a quinoline ring structure with a methyl group at position 1, a phenyl group at position 2, and a methoxy group at position 6. 6-methoxy-1-methyl-2-phenyl-4(1H)-quinolinone is known for its potential applications in the pharmaceutical and chemical industries, particularly as a precursor in the synthesis of various drugs and other organic compounds. Its chemical structure and properties make it an interesting target for researchers studying the synthesis and reactivity of quinolinone derivatives.

6878-08-6

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6878-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6878-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6878-08:
(6*6)+(5*8)+(4*7)+(3*8)+(2*0)+(1*8)=136
136 % 10 = 6
So 6878-08-6 is a valid CAS Registry Number.

6878-08-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Eduline

1.2 Other means of identification

Product number -
Other names 6-Methoxy-1-methyl-2-phenyl-1H-quinolin-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6878-08-6 SDS

6878-08-6Downstream Products

6878-08-6Relevant academic research and scientific papers

Rat small intestine muscle relaxation alkaloids from Orixa japonica leaves

Funayama, Shinji,Tanaka, Rioko,Kumekawa, Yasuhiro,Noshita, Toshiro,Mori, Tetsuya,Kashiwagura, Tadashi,Murata, Kiyoshi

, p. 100 - 102 (2001)

Two quinoline alkaloids, japonine (1) and eduline (2) were isolated from the methanol extract of the leaves of Orixa japonica as relaxants against rat small intestine muscle. The activity of these alkaloids was comparable to that of the typical muscle rel

Direct Synthesis of 4-Quinolones via Copper-Catalyzed Anilines and Alkynes

Xu, Xuefeng,Zhang, Xu

supporting information, p. 4984 - 4987 (2017/09/22)

A unique and direct approach for constructing 4-quinolones from simple and readily available anilines and alkynes is described. Under the optimal conditions, both N-alkyl- and N-aryl-substituted anilines can be successfully transformed into the corresponding 4-quinolones. This reaction is characterized by mild reaction conditions, high functional-group tolerance, and amenability to gram-scale synthesis.

Short step synthesis of natural 2-arylquinolones based on iridium-catalyzed three-component coupling quinoline synthesis

Nakajima, Takayuki,Inada, Takashi,Shimizu, Isao

, p. 497 - 504 (2008/02/03)

Eduline (la), graveoline (1b), and 6-methoxy-2-(4-methoxyphenyl)-1-methylquinolone (1c) were synthesized by iridium-catalyzed three-component coupling reaction. Reaction of an aniline, an aromatic aldehyde, and acetaldehyde gave the corresponding substitu

Synthesis of 2-arylquinoline and 2-aryl-4-quinolone alkaloids via Diels- Alder reaction of 1,2,3-benzotriazine with enamines

Koyama, Junko,Toyokuni, Izumi,Tagahara, Kiyoshi

, p. 1038 - 1039 (2007/10/03)

Synthesis of the 2-arylquinoline alkaloids, 2-phenylquinoline and dubamine, and the 2-arylquinolone alkaloids, 1-methyl-2-phenyl-4-quinolone, graveoline, reevesianine-A, and eduline, was accomplished by the Diels-Alder reaction of 1,2,3-benzotriazine with enamines as a key step.

The Chemistry of 2H-3,1-Benzoxazine-2,4(1H)-dione (Isatoic Anhydride). 9. Synthesis of 2-Arylquinoline Alkaloids

Coppola, Gary M.

, p. 727 - 731 (2007/10/02)

A one-step synthesis of N-methyl-2-aryl-4-quinolone alkaloids is described.These compounds are readily prepared from the reaction of an N-methylisatoic anhydride with the lithium enolate of an acetophenone.By this method, the reaction of N-methylisatoic a

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