Scholarly article on 1-methylbenzo[f]quinolin-3(4H)-one 3919-50-4 from Journal of the American Chemical Society p. 644,645

DOI: 10.1021/ja01208a035

Source and publish data:

Journal of the American Chemical Society p. 644,645 (1946)

Update date:2022-08-02

Topics:

Authors:

Kaslow Kaslow

Sommer Sommer

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/ja01208a035

Full text of DOI:10.1021/ja01208a035

Products guided by the article

Product name:1-methylbenzo[f]quinolin-3(4H)-one

Cas No:3919-50-4

R&D Labs maybe for 3919-50-4

Amadis Chemical Co., Ltd.

website:http://www.amadischem.com

Contact:86-571-89925085

Address:Watts Cosine.No.166.Xiangmao Road.
Zhushan County Tianxin Pharmaceutical & Chemical Co., Ltd.

Contact:0086-719-4224892

Address:Tutang Road, Chengguan Town, Zhushan County, Hubei Province
HAORUI ENTERPRISES LLC

Contact:(1) 206-3550089

Address:5115 NE 8TH PL, Renton, WA 98059 USA
TIANJIN FESTO CHEMICAL CO.,LTD(expird)

Contact:86-22-25814570

Address:No.12th,5th Ave.,TEDA,Tianjin,China
Shanghai PengMo Biotechnology Co.,Ltd

website:http://www.pengmobio.lookchem.com

Contact:86-13052359378

Address:No.218 Hai Qu Road.Shanghai.China

Relevant to this article

[3+2] and [4+1] cycloaddition reactions of fischer alkoxy(alkenyl)carbene complexes with electronically neutral 1,3-dienes

Doi:10.1002/anie.200390087
(2003)
A genetically encoded ¹⁹F NMR probe for tyrosine phosphorylation

Doi:10.1002/anie.201300463
(2013)
Bis(2-(acylamino)phenyl) disulfides, 2-(acylamino)benzenethiols, and S-(2-(acylamino)phenyl) alkanethioates as novel inhibitors of cholesteryl ester transfer protein

Doi:10.1021/jm000224s
(2000)
α-Carboxy-β-lactones from photoinduced ring contraction of 3-diazodihydrofuran-2,4-diones

Doi:10.1055/s-0032-1316860
(2013)
Antimitotic Agents: Structure-Activity Studies with Some Pyridine Derivatives

Doi:10.1021/jm00098a014
(1992)
Direct carboxamidation of sydnones with chlorosulfonyl isocyanate

Doi:10.1080/00032719808006493
(1998)

Article Doi

DOI: 10.1021/ja01208a035