Synthesis and characterization of [phenyl-3H] clonidine hydrochloride at high specific activity

DOI: 10.1002/jlcr.457

Source and publish data:

Journal of labelled compounds and radiopharmaceuticals p. 323 - 327 (2001)

Update date:2022-08-02

Topics:

Authors:

Filer, Crist N.

Ahern, David G.

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

Article abstract of DOI:10.1002/jlcr.457

p-Aminoclonidine hydrochloride 1 was converted to m-dibromo-p-iodoclonidine 3 and the latter was used as a precursor to prepare [phenyl-³H] clonidine hydrochloride 4 at high specific activity via a selective catalytic dehalogenation with tritiu

Full text of DOI:10.1002/jlcr.457

Products guided by the article

Product name:m-dibromo-p-iodoclonidine

Cas No:101377-49-5

R&D Labs maybe for 101377-49-5

Ningbo Hi-tech Zone Nice-Synth Chemical Industry Ltd.

Contact:+86-(574)-81110986

Address:No. 1210, Building 3, Wante Business Centre, Hi-tech Zone, Ningbo
Jinan Kaypharm Chemical Co.,Ltd

Contact:86-0531-86986780

Address:Room101,No189-2,Huayuan Road,Jinan City,Shandong Province
Dalian RSD International Trade Co.,Ltd.(expird)

Contact:86-22-60875058 58610575

Address:Wantong International Areas, Hongqiao District, Tianjin, China.China
Dongying J&M Chemical Co., Ltd,

Contact:546-8551108

Address:Room 1219, Zisheng Mansion, Zibo Road, Dongying, Shandong, China
ZCIC INTERNATIONAL LTD

Contact:+86-512-56795332

Address:No227 Shuanglong Rd, Fenghuang, Zhangjiagang

Relevant to this article

New steroid-fused P-heterocycles. Part II. Synthesis and conformational study of oxazaphosphorino[16,17-e]estrone derivatives

Doi:10.1016/j.steroids.2007.02.001
(2007)
Development of a novel NURR1/NOT agonist from hit to lead and candidate for the potential treatment of Parkinson's disease

Doi:10.1016/j.bmcl.2019.01.024
(2019)
Doi:10.1021/jo01029a070
(1964)
The Use of Chloroformamidine Hydrochloride as a Reagent for the Synthesis of Guanidines from Electron Deficient Aromatic Amines

Doi:10.1002/jhet.2567
(2017)
Doi:10.1039/jr9600002674
(1960)
A Tandem Enzymatic sp²-C-Methylation Process: Coupling in Situ S-Adenosyl-l-Methionine Formation with Methyl Transfer

Doi:10.1002/cbic.201700115
(2017)

Article Doi