Scholarly article on Cl2(P(CH3)2C6H5)2MoWCl2(P(CH3)2C6H5)2 109215-61-4 from Journal of the American Chemical Society p. 7978 - 7979

DOI: 10.1021/ja00337a058

Source and publish data:

Journal of the American Chemical Society p. 7978 - 7979 (1984)

Update date:2022-07-31

Topics:

Authors:

Luck, Rudy L.

Morris, Robert H.

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

Article abstract of DOI:10.1021/ja00337a058

Full text of DOI:10.1021/ja00337a058

Products guided by the article

Product name:Cl₂(P(CH₃)2C₆H₅)2MoWCl₂(P(CH₃)2C₆H₅)2

Cas No:109215-61-4

R&D Labs maybe for 109215-61-4

JIANGSU GRAND XINYI PHARMACEUTICAL CO.,LTD

website:http://www.xypharm.com/

Contact:+86-515-84383317

Address:Chenli Road,Costal Chemical Area Binhai,Yancheng, Jiangsu,China
jiangsu hualin chemical co.,ltd.

Contact:86-25-87787402

Address:jaingsu,china
Hangzhou JINLAN Pharm-Drugs Technology Co., Ltd

website:http://www.jlpharms.com

Contact:86-571-86982636

Address:Rm A606, Fuyi Center, jianqiao street
ZHIJIANG ZENVA SINO COMMERCE AND TRADE CO., LTD.

website:http://www.zenvasino.com

Contact:+86-138-72658998

Address:Shibeishan Road,Zhijiang, Hubei, China
Nanyang Tianhua pharmaceutical Co.,Ltd.

Contact:+8618639816203

Address:Longsheng Industrial Park

Relevant to this article

Design and synthesis of 1H-indazole-3-carboxamide derivatives as potent and selective PAK1 inhibitors with anti-tumour migration and invasion activities

Doi:10.1016/j.ejmech.2020.112517
(2020)
Doi:10.1007/BF00901130
(1959)
Doi:10.1021/jo01133a010
(1953)
Na₂S₂O₄: A versatile reagent for the one-pot synthesis of 2-aryl-1h-imidazo[4,5-c]pyridines from 4-amino-3- nitropyridine and aldehydes via reductive cyclization

Doi:10.1080/00397910903011345
(2010)
Amino-sugar modular ligands - Useful cores for the formation of asymmetric copper 1,4-addition catalysts

Doi:10.1039/b813137f
(2008)
A potent and selective C-11 labeled PET tracer for imaging sphingosine-1-phosphate receptor 2 in the CNS demonstrates sexually dimorphic expression

Doi:10.1039/c5ob00951k
(2015)

Article Doi

DOI: 10.1021/ja00337a058