New compounds: synthesis of 3,4,5 trimethoxybenzenesulfonamides

DOI: 10.1002/jps.2600620847

Source and publish data:

Journal of Pharmaceutical Sciences p. 1392 - 1394 (1973)

Update date:2022-08-05

Topics:

Authors:

Pifferi Pifferi

Monguzzi

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

Article abstract of DOI:10.1002/jps.2600620847

Full text of DOI:10.1002/jps.2600620847

Products guided by the article

Product name:2,3,4-trimethoxybenzenesulfonic acid

Cas No:42771-31-3

R&D Labs maybe for 42771-31-3

Buffett (China) Holding Co.,Ltd

Contact:4006570891

Address:
Hefei EnliPharma Tecnology Co.,Ltd

Contact:0086-551-66399836

Address:Qing Cheng ShuiXiang Building 805, Mengcheng North Road , ShuangFeng Economic Development Zone Anhui HeFei
FOSHAN NANHAI ZHONGNAN PHARMACEUTICAL FACTORY

Contact:0086-0757-85609331

Address:XIAHENGTIAN INDUSTRIAL ZONE,SHAYONG VILLAGE,LISHUI TOWN
Kunming Biohome Technology Co. Ltd.

website:http://www.biohometech.com/

Contact:86-871-67428869

Address:kunming
Phytomarker Ltd.(expird)

Contact:+86-22-26358246

Address:601-4-20, Fujiayuan, Tiantai Road, Hebei District, Tianjin, China

Relevant to this article

The regio- and stereoselective addition of carbon nucleophiles to trifluoromethyl phenylsulfanyl acetylene: A novel and expeditious approach to 3-trifluoromethyl furans

Doi:10.1016/S0040-4039(01)02230-4
(2002)
Generation of Tertiary Phosphine-Coordinated Pd(0) Species from Pd(OAc)2 in the Catalytic Heck Reaction

Doi:10.1246/cl.1992.2177
(1992)
Azido-Functionalized Aromatic Phosphonate Esters in ^RPOSS-Cage-Supported Lanthanide Ion (Ln = La, Nd, Dy, Er) Coordination

Doi:10.1021/acs.inorgchem.1c00266
(2021)
Synthesis of some novel 4-imino-3,5,7-trisubstituted pyrido[2,3-d]pyrimidine-2(1H)-thiones and their nucleosides as potential therapeutic agents

Doi:10.1080/10426500008076330
(2000)
Doi:10.1002/hlca.19730560324
(1973)
The Conjugate Addition of Glyoxalate-Derived Anion Equivalents by Phase Transfer Catalysis

Doi:10.1055/s-1983-30563
(1983)

Article Doi