Scholarly article on 1-Isopropyl-2-methoxy-4-[(E)-2-((S)-2,6,6-trimethyl-cyclohex-2-enyl)-vinyl]-benzene 69999-68-4 from Bulletin of the Chemical Society of Japan p. 212 - 215

DOI: 10.1246/bcsj.52.212

Source and publish data:

Bulletin of the Chemical Society of Japan p. 212 - 215 (1979)

Update date:2022-08-02

Topics:

Authors:

Matsumoto,T.

Usui,S. Usui,S.

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

Article abstract of DOI:10.1246/bcsj.52.212

Full text of DOI:10.1246/bcsj.52.212

Products guided by the article

Product name:1-Isopropyl-2-methoxy-4-[(E)-2-((S)-2,6,6-trimethyl-cyclohex-2-enyl)-vinyl]-benzene

Cas No:69999-68-4

R&D Labs maybe for 69999-68-4

Huangshan Violet Biological Technology Co., Ltd

Contact:+86-559-2335676

Address:16-201 JinShanYuan,JiangNan New City,TunXi District,HuangShan City,AnHui Province,China
Mollt Biochem Co., Ltd(expird)

Contact:+86-21-38682181

Address:shanghai ,china
Shanghai UCHEM Inc.

Contact:+86-21-56338808

Address:799 Dunhuang Road, Putuo
Allicon Pharmaceuticals,Inc.

Contact:+86-519-86339586，13584329896

Address:Changzhou Scientific and Education Park
Cangzhou Senary Chemical Science-tech Co., Ltd

Contact:+86-317-3563899, 3563699

Address:168 Jinde Road, Cangzhou, Hebei, China

Relevant to this article

α-Oxoketene dithioacetals mediated heteroaromatic annulation protocol for benzoheterocycles: An efficient regiocontrolled synthesis of highly substituted and annulated indazoles

Doi:10.1016/j.tet.2004.02.029
(2004)
Doi:10.1039/jr9360001598
(1936)
PhBCl₂ promoted reductive opening of 2′,4′-O-p- methoxybenzylidene: New regioselective differentiation of position 2′ and 4′ of α-L-iduronyl moieties in disaccharide building blocks

Doi:10.1016/j.tetlet.2004.03.046
(2004)
Visible-light mediated trifluoromethylation of p-quinone methides by 1,6-conjugate addition using pyrylium salt as organic photocatalyst

Doi:10.1016/j.tet.2019.06.029
(2019)
Modulation of photochemical damage in normal and malignant cells by naturally occurring compounds

Doi:10.1111/j.1751-1097.2012.01156.x
(2012)
Design, synthesis and biological evaluation of novel nitroaromatic compounds as potent glutathione reductase inhibitors

Doi:10.1016/j.bmcl.2011.07.002
(2011)

Article Doi

DOI: 10.1246/bcsj.52.212