Scholarly article on 1,6-dichloro-1,6-bis-(4-methoxy-phenyl)-hexane 58819-39-9 from Journal of the American Chemical Society p. 3313,3316

DOI: 10.1021/ja01178a012

Source and publish data:

Journal of the American Chemical Society p. 3313,3316 (1949)

Update date:2022-07-29

Topics:

Authors:

Mueller Mueller

May May

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

Article abstract of DOI:10.1021/ja01178a012

Full text of DOI:10.1021/ja01178a012

Products guided by the article

Product name:1,6-dichloro-1,6-bis-(4-methoxy-phenyl)-hexane

Cas No:58819-39-9

R&D Labs maybe for 58819-39-9

Hangzhou JINLAN Pharm-Drugs Technology Co., Ltd

website:http://www.jlpharms.com

Contact:86-571-86982636

Address:Rm A606, Fuyi Center, jianqiao street
Changzhou Sunsheng Chem Co., Ltd

Contact:+1-(989)-854-0648

Address:No. 28 Yinshan Rd., Xixiashu Industrial Park
Jiangsu Allyrise Pharmaceutical Co., Ltd.(expird)

Contact:+86-523-86818997

Address:Taizhou,Jiangsu Province,CHINA
Shandong Topscience Biotech Co., Ltd.

Contact:0633-2619278

Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China
Brichem ( Haikou ) Co. Ltd.

Contact:86-898-65311214

Address:Room 102, BLDG. 68 Jiangnan City, No. 66 Heping Road,Haikou, Hainan, China

Relevant to this article

One-stage procedure of synthesis of highly reactive α-chloro-β- ketoacetals. 4-chloropyrazoles from α-chloro-β-ketodimethoxyacetals

Doi:10.1134/s1070428008020024
(2008)
Round-Trip Oxidative Addition, Ligand Metathesis, and Reductive Elimination in a P^III/P^VSynthetic Cycle

Doi:10.1021/jacs.0c07580
(2020)
Preparation of 3,4,5-substituted furan-2(5H)-ones using aluminum hydrogen sulfate as an efficient catalyst

Doi:10.1016/j.crci.2013.06.009
(2014)
A formal anti-Markovnikov hydroalkoxylation of allylic alcohols with a ruthenium catalyst

Doi:10.1246/cl.171104
(2018)
Structure-based design of highly selective β-secretase inhibitors: Synthesis, biological evaluation, and protein-ligand x-ray crystal structure

Doi:10.1021/jm3008823
(2012)
Enantioselective total synthesis of (+)-lithospermic acid

Doi:10.1021/ol302273r
(2012)

Article Doi

DOI: 10.1021/ja01178a012