Studies on pyridazines. XXIII. Synthesis of N substituted 1,4 dihydropyridazines

DOI: 10.1248/cpb.22.2894

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2894 - 2897 (1974)

Update date:2022-08-03

Topics:

Authors:

Kaneko Kaneko

Tsuchiya

Igeta Igeta

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

Article abstract of DOI:10.1248/cpb.22.2894

Full text of DOI:10.1248/cpb.22.2894

NII-Electronic Library Service

Products guided by the article

Product name:3-phenyl-4H-pyridazine-1-carboxylic acid methyl ester

Cas No:55307-01-2

R&D Labs maybe for 55307-01-2

Hybio Pharmaceutica Co.,Ltd

website:http://www.hybio.com.cn

Contact:+86 755 26588093

Address:No.9 Linkong West Street, Hengdian Street, Huangpi District, Wuhan City, China.
Yurui(Shanghai)Chemical Co.,Ltd

Contact:0086 21-50456736

Address:No.3188 Xiupu Road,Shanghai
LinHai Cina Chemical Co., LTD.

Contact:0576-85580989

Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China
Zibo Linzi Darong Fine Chemical Co., Ltd(expird)

Contact:86-532-67773200; 15689126900

Address:Qidu town,Linzi district,Zibo city,Shandong province,China
Sanming Coffer Fine Chemical Industrial Co., Ltd

website:http://www.cofferxm.com/

Contact:+86-598-5853979

Address:Jin-sha Yuan Chuang-ye Park,Hi-Tech Development Zone,Sanming City P.R.China

Relevant to this article

Macrocyclic polyfunctional lewis bases-VI¹ 1 Part V: A. Cygan and J.F. Biernat, Polish J. Chem. in press. Polyoxaferrocenophanes

Doi:10.1016/0040-4020(80)80232-8
(1980)
One-Pot Synthesis of Indoles and Pyrazoles via Pd-Catalyzed Couplings/Cyclizations Enabled by Aqueous Micellar Catalysis

Doi:10.1021/acs.orglett.0c02315
(2020)
N-butyl-N-methyl-11-(3'-hydroxy-21',17'-carbolactone-19'-nor-17'α- pregna-1',3',5'(10')-trien-7'α-yl)-undecanamide: An inhibitor of type 2 17β-hydroxysteroid dehydrogenase that does not have oestrogenic or androgenic activity

Doi:10.1016/S0223-5234(00)00124-0
(2000)
Glucoselysine is derived from fructose and accumulates in the eye lens of diabetic rats

Doi:10.1074/jbc.RA119.010744
(2019)
Doi:10.1016/S0040-4020(01)97120-0
(1974)
Doi:10.1039/c39750000045
(1975)

Article Doi