Scholarly article on 1-acetyl-2-(2-methyl-anilino)-2,3-dihydro-indole 38627-49-5 from Journal of the Chemical Society. Chemical communications p. 1067

DOI: 10.1039/C3972001067a

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1067 (1972)

Update date:2022-07-29

Topics:

Authors:

Forrest Forrest

Chen Chen

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

Article abstract of DOI:10.1039/C3972001067a

Full text of DOI:10.1039/C3972001067a

View Article Online / Journal Homepage / Table of Contents for this issue

Products guided by the article

Product name:1-acetyl-2-(2-methyl-anilino)-2,3-dihydro-indole

Cas No:38627-49-5

R&D Labs maybe for 38627-49-5

Shanghai shibo Chemical Co., Ltd

Contact:+86-021-60753516

Address:688 Qiushi Road, Jinshan High-tech Park, Shanghai, China,201512
Tianjin Ingenochem Technology Co.,Ltd

Contact:+86-22-23677060

Address:Hitech Green Industry Park K2-9-602, Nankai district
Changyi Xinxing Technology Development Co., Ltd.

Contact:0086-510-86651065(Time Zone:8),86651656

Address:94 Yingbinxilu WestRoad, Huangtu Town, Jiangyin City, Jiangsu, China
Jinhua Haoyuan Chemical CO., LTD(expird)

Contact:86-579-82465583

Address:Jinhua,Zhejiang
Guangxi Shanyun Biochemical Science and Technology Co., Ltd

Contact:+86-0772--6828887

Address:#2 Industrial Park of Luzhai County, Liuzhou, Guangxi, China

Relevant to this article

Doi:10.1021/ic50124a001
(1973)
Doi:10.1111/j.1432-1033.1977.tb11425.x
(1977)
Doi:10.1039/C39720001260
(1972)
Synthesis and fluorescence emission behavior of anti-[2.3](3,10)phenanthrenophane: Overlap between phenanthrene rings required for excimer formation

Doi:10.1246/cl.2001.970
(2001)
Intramolecular Diels-Alder reactions of N-alkenyl-2(1H)-pyrazinones: Generation of a novel type of cis-1,7-naphthyridine

Doi:10.1016/S0040-4039(01)01545-3
(2001)
Aminomethyl-substituted ferrocenes and derivatives: Straightforward synthetic routes, structural characterization, and electrochemical analysis

Doi:10.1021/om400317s
(2013)

Article Doi

DOI: 10.1039/C3972001067a