Scholarly article on 2,5-dimethyl-1-(2-trifluoromethyl-phenyl)-4,5-dihydro-1H-imidazole 40366-89-0 from Journal of the Chemical Society. Perkin transactions I p. 453 - 456

DOI: 10.1039/P19730000453

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 453 - 456 (1973)

Update date:2022-08-03

Topics:

Authors:

Partridge,M.W.

Smith,A.

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

Article abstract of DOI:10.1039/P19730000453

Full text of DOI:10.1039/P19730000453

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:2,5-dimethyl-1-(2-trifluoromethyl-phenyl)-4,5-dihydro-1H-imidazole

Cas No:40366-89-0

R&D Labs maybe for 40366-89-0

Purestar Chem Enterprise Co.,Ltd

website:http://www.purestarchem.com

Contact:05722157374

Address:no235.huanchengdong Rd
Beijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)

Contact:010-52876516

Address:tongzhoubeiyuan
Hefei Highzone Fine Chemical S&T CO.,LTD

Contact:86-0551-63663560

Address:room 1801 NO. 24 Shuguang RD.
Xuzhou Tianrun Chemical Co.,Ltd

website:http://www.tianrunchem.cn

Contact:86-516-83832636

Address:fuxing road
ShenZhen InnoSyn Biotech Co.,Ltd

website:http://www.innosyns.com

Contact:+86-755-28351685

Address:Floor 5 & 6, Building A1, HAIKEXING Strategic Innovative Industrial Park, 16 BaoShan Road, PingShan District

Relevant to this article

Doi:10.1007/BF00471518
()
Synthesis and anticoccidial activity of 3-fluoro-5-chloro- and -bromo-2,6-dimethyl-4-pyridinol.

Doi:10.1021/jm00261a033
(1973)
Synthesis of N -arylisatins by the reaction of arynes with methyl 2-Oxo-2-(arylamino)acetates

Doi:10.1021/jo200651b
(2011)
Doi:10.1002/zaac.19744030107
(1974)
Synthesis of 1,8-diborylnaphthalenes by the ring-opening reaction of a new anionic boron-bridged naphthalene derivative

Doi:10.1021/om010946x
(2002)
Design, synthesis, insecticidal, and acaricidal activities of novel pyrimidinamine derivatives containing a biphenyl ether

Doi:10.1002/jhet.3710
(2019)

Article Doi

DOI: 10.1039/P19730000453