Scholarly article on TELLURIUM HEXAFLUORIDE 7783-80-4 from Journal of the American Chemical Society p. 885 - 885

DOI: 10.1021/ja01330a004

Source and publish data:

Journal of the American Chemical Society p. 885 - 885 (1933)

Update date:2022-08-29

Topics:

Authors:

Yost, D. M.

Claussen, W. H.

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

Article abstract of DOI:10.1021/ja01330a004

Full text of DOI:10.1021/ja01330a004

Products guided by the article

Product name:TELLURIUM HEXAFLUORIDE

Cas No:7783-80-4

R&D Labs maybe for 7783-80-4

Hebei Tete Trade Co., Ltd.

Contact:86-311-83160559

Address:shijiazhuang
Changzhou Screw International Trading Co., Ltd.

Contact:13906149256,18001495888

Address:Jiangsu，Jintanqu
Shandong Ailitong New Material Co.,Ltd

Contact:+86-536-3226266

Address:zhongjia village, putong town , qingzhou city,Shandong Province,China
Xiamen Goodhealth Pharmchem Co., Ltd.

Contact:0086-592-2097683

Address:404R No.2 54# Minzu Rd., Xiamen, China
Zhengzhou Minzhong Pharmaceutical Co.,ltd

Contact:0086-371-65797115

Address:15/F,Jiangshan Bldg, NO.126 Huanghe Road,Zhengzhou, China

Relevant to this article

A general strategy for development of a single benzene fluorophore with full-color-tunable, environmentally insensitive, and two-photon solid-state emission

Doi:10.1039/c9cc06260b
(2019)
Microwave-assisted clean synthesis of xanthenes and chromenes in [bmim][PF₆] and their antioxidant studies

Doi:10.1007/s11164-014-1821-4
(2015)
Synthesis of symmetrical dinitro-and diamino-substituted Troeger's base analogues

Doi:10.1002/ejoc.201201188
(2012)
Reexamination of the Alleged Vinyl Ether Hydrolysis. Reaction of 9-Methoxy-1-oxacyclonon-2-ene: Disproof of Reversible Carbon Protonation

Doi:10.1021/ja00246a050
(1987)
Difluorocarbene chemistry: Synthesis of gem-difluorocyclopropenylalkynes and 3,3,3′,3′-tetrafluorobicyclopropyl-1,1′-dienes

Doi:10.1016/j.jfluchem.2004.10.012
(2005)
An artificial synthetic pathway for acetoin, 2,3-butanediol, and 2-butanol production from ethanol using cell free multi-enzyme catalysis

Doi:10.1039/c7gc02898a
(2018)

Article Doi

DOI: 10.1021/ja01330a004