Scholarly article on hexa-N-ethyl-N,N'-(β,β'-peroxy-di-phenethyl)-di-ammonium; diiodide 124111-72-4 from Journal of the American Chemical Society p. 5573,5581

DOI: 10.1021/ja01530a016

Source and publish data:

Journal of the American Chemical Society p. 5573,5581 (1959)

Update date:2022-08-03

Topics:

Authors:

Trifan Trifan

Bartlett

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

Article abstract of DOI:10.1021/ja01530a016

Full text of DOI:10.1021/ja01530a016

Products guided by the article

Product name:hexa-N-ethyl-N,N'-(β,β'-peroxy-di-phenethyl)-di-ammonium; diiodide

Cas No:124111-72-4

R&D Labs maybe for 124111-72-4

Luoyang Aoda chemical Co.,Ltd.

Contact:+86-379-67518785 67516588

Address:MiaoWan industry district,YanShi City,Henan,China
HANGZHOU YUNUO CHEMICAL CO.,LTD

website:http://www.yunuochem.com

Contact:0571-83715115

Address:hangzhou
Jiangxi Biochem Co.,Ltd

Contact:86-791-86629460

Address:1-6F, 118 Xinzhou road, Nanchang, Jiangxi, China
Wuxi Morality Chemical Co., Ltd(expird)

Contact:

Address:B/7F, 321th WuYun Rd, Wanda Plaza, Wuxi City, 214174, China
Shanghai AoBo Bio-Pharmaceutical Technology Co., Ltd.

Contact:+86-21-51320130-801, 816

Address:Room 601, No. 1011, Halei Road, Zhangjiang High-Tech Park, Pudong, Shanghai

Relevant to this article

Convergent synthesis of trisubstituted Z -allylic esters by wittig-schlosser reaction

Doi:10.1021/ol101843q
(2010)
Periselectivity switch of acylketenes in cycloadditions with 1-azadienes: Microwave-assisted diastereoselective domino three-component synthesis of α-spiro-Δ-lactams

Doi:10.1021/ol101938r
(2010)
Organocatalytic asymmetric synthesis of chiral pyrrolizines by cascade conjugate addition-aldol reactions

Doi:10.1021/ol101811c
(2010)
Self-assembly and host-guest interaction of metallomacrocycles using fluorescent dipyrazole linker with dimetallic clips

Doi:10.1021/ic100724r
(2010)
Design, synthesis and herbicidal activity study of aryl 2,6-disubstituted sulfonylureas as potent acetohydroxyacid synthase inhibitors

Doi:10.1016/j.bmcl.2017.06.007
(2017)
Doi:10.1021/ja01864a035
(1940)

Article Doi

DOI: 10.1021/ja01530a016