Scholarly article on Benzene, 1-fluoro-4-(2,3,3-trichloro-1-cyclopropen-1-yl)- 3854-79-3 from Journal of the American Chemical Society p. 4215

DOI: 10.1021/ja01073a075

Source and publish data:

Journal of the American Chemical Society p. 4215 - 4216 (1964)

Update date:2022-08-30

Topics:

Authors:

Tobey,S.W.

West,R. West,R.

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

Article abstract of DOI:10.1021/ja01073a075

Full text of DOI:10.1021/ja01073a075

Products guided by the article

Product name:Benzene, 1-fluoro-4-(2,3,3-trichloro-1-cyclopropen-1-yl)-

Cas No:3854-79-3

R&D Labs maybe for 3854-79-3

Shanghai Balmxy Pharmaceutical Co., Ltd

Contact:0086-21-24206007

Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China
SHIFANG SUHONG CHEMICAL CO.,LTD

Contact:+86-838-2224563

Address:Room 1207 Zongchen Sunshine No.128 Taishan South Road,Deyang City,Sichuan China
Lanzhou SchiffChem Co.,Ltd

Contact:86-931-8272767

Address:Room 602, No.461, Nanchang Road, Chengguan District, Lanzhou City, China PRC
Accendatech Co., LTD

Contact:+86-22-83718541

Address:32th Floor, Rongqiao Center Intersection of Changjiang Road and Nankai Six Road Nankai District Tianjin 300102, China
Tangshan Moneide Trading Co., Ltd.

Contact:+86-315-8309571

Address:2-7-420 Jidong Building Materials Commercial Center, Tangshan, Hebei, 064000 China

Relevant to this article

Inter- and intra-molecular H-bonds induced different nanostructures from a multi-H-bonding (MHB) amphiphile: Nanofibers and nanodisks

Doi:10.1039/b402956a
(2004)
Stereocontrolled synthesis of (2S*,3R*,4R*)-4-hydroxy-3-methylproline using a silicon assisted aza-[2,3]-Wittig sigmatropic rearrangement

Doi:10.1039/b007586h
(2001)
Synthesis, characterization, DNA binding, light switch "on and off", docking studies and cytotoxicity, of ruthenium(II) and cobalt(III) polypyridyl complexes

Doi:10.1007/s10895-014-1355-6
(2014)
Selective TEMPO-Oxidation of Alcohols to Aldehydes in Alternative Organic Solvents

Doi:10.1002/ejoc.201901365
(2020)
Transition-Metal-Free CO-Releasing BODIPY Derivatives Activatable by Visible to NIR Light as Promising Bioactive Molecules

Doi:10.1021/jacs.5b10800
(2016)
Doi:10.1021/ja00464a028
(1977)

Article Doi

DOI: 10.1021/ja01073a075

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja01073a075

Full text of DOI:10.1021/ja01073a075

Products guided by the article

R&D Labs maybe for 3854-79-3

Relevant to this article

Inter- and intra-molecular H-bonds induced different nanostructures from a multi-H-bonding (MHB) amphiphile: Nanofibers and nanodisks

Stereocontrolled synthesis of (2S,3R,4R*)-4-hydroxy-3-methylproline using a silicon assisted aza-[2,3]-Wittig sigmatropic rearrangement

Synthesis, characterization, DNA binding, light switch "on and off", docking studies and cytotoxicity, of ruthenium(II) and cobalt(III) polypyridyl complexes

Selective TEMPO-Oxidation of Alcohols to Aldehydes in Alternative Organic Solvents

Transition-Metal-Free CO-Releasing BODIPY Derivatives Activatable by Visible to NIR Light as Promising Bioactive Molecules

Article Doi

DOI: 10.1021/ja01073a075

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja01073a075

Full text of DOI:10.1021/ja01073a075

Products guided by the article

R&D Labs maybe for 3854-79-3

Relevant to this article

Inter- and intra-molecular H-bonds induced different nanostructures from a multi-H-bonding (MHB) amphiphile: Nanofibers and nanodisks

Stereocontrolled synthesis of (2S*,3R*,4R*)-4-hydroxy-3-methylproline using a silicon assisted aza-[2,3]-Wittig sigmatropic rearrangement

Synthesis, characterization, DNA binding, light switch "on and off", docking studies and cytotoxicity, of ruthenium(II) and cobalt(III) polypyridyl complexes

Selective TEMPO-Oxidation of Alcohols to Aldehydes in Alternative Organic Solvents

Transition-Metal-Free CO-Releasing BODIPY Derivatives Activatable by Visible to NIR Light as Promising Bioactive Molecules

Stereocontrolled synthesis of (2S,3R,4R*)-4-hydroxy-3-methylproline using a silicon assisted aza-[2,3]-Wittig sigmatropic rearrangement