Scholarly article on PF4Cl 13637-88-2 from Journal of Fluorine Chemistry p. 201,202,204

DOI: 10.1016/S0022-1139(00)82513-0

Source and publish data:

Journal of Fluorine Chemistry p. 201,202,204 (1974)

Update date:2022-07-30

Topics:

Authors:

Sprenger

Shreeve Shreeve

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

Article abstract of DOI:10.1016/S0022-1139(00)82513-0

Full text of DOI:10.1016/S0022-1139(00)82513-0

Products guided by the article

Product name:PF₄Cl

Cas No:13637-88-2

R&D Labs maybe for 13637-88-2

Tianjin Te-An Chemtech Co., Ltd.(expird)

Contact:+86-22-65378638

Address:A5-8, No.80 Haiyun Street, TEDA
zhuzhou zhongle chemical co. ltd.

Contact:+86-0731 28228409

Address:Zhuzhou, Hunan, China
Huayi Isotopes Co.

Contact:+ 86 512 52491118

Address:1 Fuyu Road, Haiyu TownChangshu, Jiangsu, China
QINGDAO ON-BILLION INDUSTRAIL CO.,LTD

website:http://www.obn.com.cn

Contact:+86-15005320811 +86-532-80681989

Address:F35 Parkson Mansion No.44-60 Zhongshan Rd.
Deltachem(QingDao)Co.,Ltd.

Contact:+8618766299236

Address:ROOM808, BUILDING2,NO.230 SHEN ZHEN ROAD, LAOSHAN DISTRICT

Relevant to this article

Design of potent and selective hybrid inhibitors of the mitotic kinase nek2: Structure-activity relationship, structural biology, and cellular activity

Doi:10.1021/jm201683b
(2012)
N-Heterocyclic Carbene Catalyzed Highly Chemoselective Intermolecular Crossed Acyloin Condensation of Aromatic Aldehydes with Trifluoroacetaldehyde Ethyl Hemiacetal

Doi:10.1021/ol502581b
(2015)
Solvent-free one-pot synthesis of sulfonephthaleins from saccharin and phenols

Doi:10.1080/00397911.2010.535946
(2012)
EPR studies of nitrogen-centred free radicals. Part 50.¹ Unusual decomposition behaviour of isolable stable thioaminyl free radicals at high temperature

Doi:10.1039/a800163d
(1998)
The shiny side of copper: Bringing copper(i) light-emitting electrochemical cells closer to application

Doi:10.1039/d0ra03824e
(2020)
General Oxidative Aryl C-P Bond Formation through Palladium-Catalyzed Decarbonylative Coupling of Aroylhydrazides with P(O)H Compounds

Doi:10.1021/acs.orglett.9b00922
(2019)

Article Doi

DOI: 10.1016/S0022-1139(00)82513-0