Basic amides of 3,4,5-trimethoxyphenoxyacetic acid; synthesis and pharmacology of trimethophenoxamide and analogues

DOI: 10.1135/cccc19773628

Source and publish data:

Collection of Czechoslovak Chemical Communications p. 3628 - 3642 (1977)

Update date:2022-08-05

Topics:

Authors:

Protiva Protiva

Valenta Valenta

Trcka Trcka

et al. et al.

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

Article abstract of DOI:10.1135/cccc19773628

Full text of DOI:10.1135/cccc19773628

Products guided by the article

Product name:Acetonitrile, (3,4,5-trimethoxyphenoxy)-

Cas No:65876-16-6

R&D Labs maybe for 65876-16-6

QINGDAO NEW FLOURISH INTERNATIOANAL TRADE CO., LTD.

Contact:+86 532 80861829

Address:No. 1, Yinchuan East Road, 266061, Qingdao, China
Jinan Kaypharm Chemical Co.,Ltd

Contact:86-0531-86986780

Address:Room101,No189-2,Huayuan Road,Jinan City,Shandong Province
Xi'an Herbland Tech Inc.

Contact:+86-29-88710656

Address:South Tai bai Road, High Tech Development Zone, Xi'an China
Guangzhou PI & PI Biotech Inc. Ltd.

Contact:+86-20-81716320

Address:Suite 501,198 Kaiyuan Ave.,Science City, Guangzhou,China
HAORUI ENTERPRISES LLC

Contact:(1) 206-3550089

Address:5115 NE 8TH PL, Renton, WA 98059 USA

Relevant to this article

Synthetic studies on β-lactam antibiotics. XIX. Synthesis of 3'-nor-type 1-oxacephems

Doi:10.1016/S0040-4039(01)86758-7
(1979)
A synthetic route to sulfobetaine methacrylates with varying charge distance

Doi:10.1002/ejoc.201402734
(2014)
Synthesis of 1,4-diaryl-piperazine-2,5-diones: New behavior of N,N-dimethylformamide dimethyl acetal (DMFDMA)

Doi:10.1080/00397910701767098
(2008)
Electrophilic Catalysis in the Synthesis of Aryl Methyl- and Phenylphosphonochloridates

Doi:10.1134/S1070363218090025
(2018)
Reaction of biguanides and related compounds. XIV. Cyclization of amidinothioureas with some carbonyl compounds

Doi:10.1248/cpb.26.314
(1978)
Palladium-Catalyzed Allylic Amination of Homoallylic Alcohols with Amines via Carbon-Carbon Bond Cleavage

Doi:10.1055/s-0034-1380418
(2015)

Article Doi