Scholarly article on (1E,3E)-1,2,3,4-Tetraphenyl-1,3-butadiene 1608-10-2 from Journal of Organometallic Chemistry p. C23

DOI: 10.1016/S0022-328X(00)86437-2

Source and publish data:

Journal of Organometallic Chemistry p. C23 (1975)

Update date:2022-08-22

Topics:

Authors:

Eisch Eisch

Galle Galle

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

Article abstract of DOI:10.1016/S0022-328X(00)86437-2

Full text of DOI:10.1016/S0022-328X(00)86437-2

Products guided by the article

Product name:(1E,3E)-1,2,3,4-Tetraphenyl-1,3-butadiene

Cas No:1608-10-2

R&D Labs maybe for 1608-10-2

KA-SHING Business Trade Macau Co., Ltd.

Contact:00853-28430045

Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao
Tradlon Chemical Co., Ltd.

Contact:+86-710-3516804

Address:Number 83,Panggong road,Xiangcheng District,Xiangyang ,Hubei
Wuhan Shengmao Corp

website:http://www.shengmaochem.com

Contact:86-27-82853423, 82819281

Address:Rm 202, A Unit Huaqiao Building No. 2, Lihuangpi Road, Wuhan, China
Puyang Willing Chemicals Co.,Ltd.

Contact:86-393-4840366

Address:Puyang Henan China
KA-SHING Business Trade Macau Co., Ltd.

Contact:00853-28430045

Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao

Relevant to this article

Mild silver-mediated geminal difluorination of styrenes using an air- and moisture-stable fluoroiodane reagent

Doi:10.1002/anie.201408812
(2014)
Synthesis and Characterization of Copper(II) and Nickel(II) Complexes of 1,5-Diamino-3-pentanol and Its Derivatives

Doi:10.1246/bcsj.55.2404
(1982)
Enantioselective Access to 1H-Isoindoles with Quaternary Stereogenic Centers by Palladium(0)-Catalyzed C?H Functionalization

Doi:10.1002/anie.201809173
(2018)
Synthesis and characterization of a novel indoline based nonlinear optical chromophore with excellent electro-optic activity and high thermal stability by modifying the π-conjugated bridges

Doi:10.1039/c7tc00735c
(2017)
Contribution of pyrrole formation and polymerization to the nonenzymatic browning produced by amino-carbonyl reactions

Doi:10.1021/jf991090y
(2000)
Aqueous-phase hydrodeoxygenation of carboxylic acids to alcohols or alkanes over supported Ru catalysts

Doi:10.1016/j.molcata.2011.10.015
(2011)

Article Doi

DOI: 10.1016/S0022-328X(00)86437-2