Methyl- and Phenyl-mercury(II) Derivatives of 2-Mercaptopyridine. Crystal and Molecular Structure of Methyl(pyridine-2-thiolato)mercury(II)

DOI: 10.1039/DT9860001945

Source and publish data:

Journal of the Chemical Society, Dalton Transactions p. 1945 - 1948 (1986)

Update date:2022-08-03

Topics:

Authors:

Castineiras, Alfonso

Hiller, Wolfgang

Straehle, Joachim

Bravo, Jorge

Casas, Jose S.

et al. et al.

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

Article abstract of DOI:10.1039/DT9860001945

The compounds (R=Me or Ph, L=pyridine-2-thiolate) have been isolated by reaction of HL with methylmercury(II)hydroxide and phenylmercury(II)acetate, respectively.The crystal structure of the methyl derivative has been determined at 190 K.The comp

Full text of DOI:10.1039/DT9860001945

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

View Article Online

Products guided by the article

Product name:phenyl(pyridine-2-thiolato)mercury(II)

Cas No:76448-86-7

R&D Labs maybe for 76448-86-7

UNION PHARMPRO CO.,LTD

Contact:18710867521(wechat)

Address:Rm10516,Galaxy Tech Building #2,No.25 Tangyan Rd,Hi-Tech Zone,Xi'an, China
Jiangsu Zenji Pharmaceuticals LTD

Contact:+86-025-83172562; +1-224-888-1133(USA)

Address:No.5 Xinmofan Road
Skyrun Industrial Co.,Ltd(expird)

website:http://www.chinaskyrun.com

Contact:0086-576-84610586

Address:Chemical Development Zone
Wuhan Konberd Biotech Co., Ltd.

Contact:+86-27-87205925

Address:NO.666, Gaoxin Road, Eastlake High-tech zone
Taiwan Surfactant Corp.

Contact:886 2 2541 0022

Address:8 Fl., No. 11, Sec. 1, Chung Shan North Rd., Taipei, Taiwan R.O.C.

Relevant to this article

A new approach to the synthesis of N,N-dialkyladenine derivatives

Doi:10.1002/ejoc.200700416
(2007)
Doi:10.1021/jo01279a095
(1967)
Evidence for separate binding and scaffolding domains in the immunosuppressive and antitumor marine natural product, pateamine A: Design, synthesis, and activity studies leading to a potent simplified derivative

Doi:10.1021/ja040065s
(2004)
12-Oxo-LTB₄, a key pivotal intermediate in LTB₄ metabolism

Doi:10.1021/jo00111a044
(1995)
Doi:10.1016/S0031-9422(00)86148-8
(1965)
Largely blue-shifted emission through minor structural modifications: Molecular design, synthesis, aggregation-induced emission and deep-blue OLED application

Doi:10.1039/c3cc49313j
(2014)

Article Doi