Scholarly article on 1,2,4,6-tetraphenyl-piperazine 16076-29-2 from Bulletin of the Chemical Society of Japan p. 1896,1899

DOI: 10.1246/bcsj.44.1896

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1896,1899 (1971)

Update date:2022-08-05

Topics:

Authors:

Tsuge Tsuge

Mataka Mataka

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

Article abstract of DOI:10.1246/bcsj.44.1896

Full text of DOI:10.1246/bcsj.44.1896

Products guided by the article

Product name:1,2,4,6-tetraphenyl-piperazine

Cas No:16076-29-2

R&D Labs maybe for 16076-29-2

Daqing New Century Fine Chemical Co., Ltd.(expird)

Contact:010-57126694

Address:No.39, jinxing cun, honggang district
WENZHOU M&C FOREIGN TRADE CO.,LTD.

Contact:+86-577-88862917

Address:No.8 Liming West Road,Wenzhou,zhejiang,China
Shanghai Yuantai Chemical Products Co., Ltd

Contact:021--66129803

Address:Chengyin Road,Shanghai,China
Shijiazhuang Haitian Amino Acid Co., Ltd.

Contact:+86-311-88908111

Address:Shijiazhuang Hebei province,China
Nanjing Chemzam Pharmtech Co., Ltd.

Contact:+86-25-86462165,+86-13915979898

Address:C5-1，6 Maiyue Road，Maigaoqiao，Nanjing，Jiangsu，China

Relevant to this article

Synthesis of a type-VIβ-turn peptide mimetic and its incorporation into a high-affinity somatostatin receptor ligand

Doi:10.1002/hlca.19950780614
(1995)
Synthesis, characterization, and biological activities of some novel thienylpyrido[3′,2′:4,5]thieno[3,2-d]pyrimidines and related heterocycles

Doi:10.1002/jhet.4310
(2021)
Tuning the photophysical and electrochemical properties of iridium(III) 2-aryl-1-phenylbenzimidazole complexes

Doi:10.1016/j.ica.2014.02.024
(2014)
Diastereo- and enantioselective michael addition of 3-substituted oxindoles to trifluoromethyl-substituted nitro olefins catalyzed by a cinchona-alkaloid-derived squaramide

Doi:10.1002/ejoc.201301457
(2014)
Stereochemistry of hydrogen peroxide - Acetic acid oxidation of ursolic acid and related compounds

Doi:10.1016/S0040-4020(01)89285-1
(1994)
Azaindolylsulfonamides, with a more selective inhibitory effect on histone deacetylase 6 activity, exhibit antitumor activity in colorectal cancer HCT116 cells

Doi:10.1021/jm401899x
(2014)

Article Doi

DOI: 10.1246/bcsj.44.1896