Noncataleptic potential neuroleptics: 2-methyl-10-(4-methylpiperazino)- and -10-[4-(2-hydroxyethyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin

DOI: 10.1135/cccc19792677

Source and publish data:

Collection of Czechoslovak Chemical Communications p. 2677 - 2688 (1979)

Update date:2022-08-05

Topics:

Authors:

Valenta Valenta

Jilek Jilek

Pomykacek

et al. et al.

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

Article abstract of DOI:10.1135/cccc19792677

Full text of DOI:10.1135/cccc19792677

Products guided by the article

Product name:1-(5-methyl-2-phenylsulfanyl-phenyl)-ethanone

Cas No:73129-53-0

R&D Labs maybe for 73129-53-0

Oren Hydrocarbons (Qingdao) Co., Ltd.

Contact:+86-532-68607667-801

Address:Room 3 # 302, No.9 Qingyun Road, Qingdao, China
Chengdu Baishixing Science and Technology Industry Co., Ltd.

website:http://www.cd-bsx.com

Contact:+86-28-88531548

Address:#217,North of Industry Road,Heshan Town,Pujiang County,Chengdu,Sichuan,China.
Huangshan Violet Biological Technology Co., Ltd

Contact:+86-559-2335676

Address:16-201 JinShanYuan,JiangNan New City,TunXi District,HuangShan City,AnHui Province,China
ShangHai BMG Chemical Co., Ltd

Contact:+86-13524845543

Address:Room 602, no 291 sikai road shanghai
RongCheng Tianyu Technology Co.,Ltd.

Contact:86-631-7519595

Address:220Ping Donghai Road RongChengCity,ShangDong Province China

Relevant to this article

Synthesis, characterization, and antioxidant activity of some new N ⁴-arylsubstituted-5-methoxyisatin-β-thiosemicarbazone derivatives

Doi:10.1007/s11164-020-04079-x
(2020)
Doi:10.1021/jm00341a004
(1963)
2-amino-3-cyanofurans as precursors for anthranilic acid derivatives

Doi:10.1055/s-1980-28925
(1980)
Thermolysis of free-radical initiators: tert-butylazocumene and its 1,3- and 1,4-bisazo and 1,3,5-trisazo analogues

Doi:10.1021/ja003914u
(2001)
HALOGENOPHILIC REACTION OF SILYLATED PHOSPHITES WITH TRICHLOROACETIC ACID DERIVATIVES

Doi:10.1007/BF00965439
(1991)
1,2,4-Thiadiazolidin-3,5-diones as novel hydrogen sulfide donors

Doi:10.1016/j.ejmech.2017.10.068
(2018)

Article Doi