Scholarly article on 3-phenyl-5-propyl-3H-benzofuran-2-one 32292-89-0 from Journal of the American Chemical Society p. 653,654

DOI: 10.1021/ja01123a021

Source and publish data:

Journal of the American Chemical Society p. 653,654 (1952)

Update date:2022-08-05

Topics:

Authors:

Weston Weston

Brownell

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

Article abstract of DOI:10.1021/ja01123a021

Full text of DOI:10.1021/ja01123a021

Products guided by the article

Product name:3-phenyl-5-propyl-3H-benzofuran-2-one

Cas No:32292-89-0

R&D Labs maybe for 32292-89-0

Shanghai Kefu Chemical Co.,Ltd.

Contact:+86-21-34616196

Address:Room601-602, Xuhui Business Building, No.168, Yude Road, Shanghai
Changzhou Foreign Trade Corp

Contact:+86-519-86623222

Address:29F/D, 99 Yanling West Road, Changzhou, Jiangsu, China
kern enterprises

Contact:+86-13236304423

Address:heping street NO.828,weifang city,shandong province,china
JiangXi Hong Run Chemical Co., Ltd

Contact:+86-0791-88521351

Address:XingHuo industrial zone in YongXiu county
ZHIJIANG ZENVA SINO COMMERCE AND TRADE CO., LTD.

website:http://www.zenvasino.com

Contact:+86-138-72658998

Address:Shibeishan Road,Zhijiang, Hubei, China

Relevant to this article

The Paal-Knorr reaction revisited. A catalyst and solvent-free synthesis of underivatized and N-substituted pyrroles

Doi:10.1039/c4gc01523a
(2015)
New palladium complexes with rigid scorpion-type ligands. Crystal structure of complexes [Pd(η³-2-CH₃-C₃H ₄)(bpz*mPh)](CF₃SO₃) and [Pd(bpz*mpy)₂](BF₄)₂. bpz*mPh=phenyl-bis(3,5-dimethylpyrazol-1-yl)methane; Bpz*mpy=pyridin-2-yl-bis(3,5-dimethylpyrazol-1-yl)methane

Doi:10.1016/S0022-328X(00)00160-1
(2000)
Three-Component Synthesis of Quinolines Based on Radical Cascade Visible-Light Photoredox Catalysis

Doi:10.1002/adsc.201800734
(2018)
Doi:10.1139/v71-265
(1971)
3-Ethenyl-5-methoxy-indole derivatives. 2. Synthesis of antiphlogistic indole derivatives

Doi:10.1002/ardp.19713040710
(1971)
Synthesis of potent non-imidazole histamine H₃-receptor antagonists

Doi:10.1002/(SICI)1521-4184(199812)331:12<395::AID-ARDP395>3.0.CO;2-7
(1998)

Article Doi

DOI: 10.1021/ja01123a021