Scholarly article on Bis--ether 23889-90-9 from Journal of the Chemical Society C: Organic p. 1515

DOI: 10.1039/j39690001515

Source and publish data:

Journal of the Chemical Society C: Organic p. 1515 (1969)

Update date:2022-07-30

Topics:

Authors:

Brooklyn

Finar Finar

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

Article abstract of DOI:10.1039/j39690001515

Full text of DOI:10.1039/j39690001515

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

View Article Online

Products guided by the article

Product name:Bis-<α-(1-phenyl-pyrazolyl-(4))-benzyl>-ether

Cas No:23889-90-9

R&D Labs maybe for 23889-90-9

MINS GROUP CO.,LIMITED

Contact:18669908765

Address:Zibo City, Shandong Province, P.R.China
SHANGHAI RC CHEMICALS CO.,LTD.

website:http://www.rcc.net.cn

Contact:+86-21-50322175

Address:Rm1415 Yinqiao Masion No.58 Jinxin Road Pudong Shanghai China
Nantong Kaixin Pharma Chemical Co.,Ltd.

Contact:86-513-85250786

Address:2-1103 Huachen Mansion, 111 Gongnong Road,Nantong, Jiangsu, China
Wuxi Zuping Food Science And Technology Co.,LTD.

Contact:+86-510-87210822

Address:Guanlin town
RongCheng Tianyu Technology Co.,Ltd.

Contact:86-631-7519595

Address:220Ping Donghai Road RongChengCity,ShangDong Province China

Relevant to this article

Crown ethers with an azo or azoxy unit and sulfur atom(s) in a 13- membered macrocycle

Doi:10.1016/S0040-4020(99)00430-5
(1999)
Ir-catalyzed preparation of SF₅-substituted potassium aryl trifluoroborates via C-H borylation and their application in the Suzuki-Miyaura reaction

Doi:10.1021/ol4025666
(2013)
Synthesis of some N-heteroaromatic analogues of cannabinoids

Doi:10.1002/jhet.5570180105
(1981)
Doi:10.1016/S0040-4039(01)88331-3
(1969)
Doi:10.1021/jo00831a062
(1970)
Chemical transformations of oxyresveratrol (trans-2,4,3′,5′-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent

Doi:10.1016/j.bmcl.2006.08.018
(2006)

Article Doi

DOI: 10.1039/j39690001515