Scholarly article on 4-Chlor-2-nitro-1--benzol 95770-04-0 from Journal of medicinal and pharmaceutical chemistry p. 389 - 397

DOI: 10.1021/jm01237a017

Source and publish data:

Journal of medicinal and pharmaceutical chemistry p. 389 - 397 (1962)

Update date:2022-07-29

Topics:

Authors:

Vaidya,M.G.

Cannon,J.G.

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

Article abstract of DOI:10.1021/jm01237a017

Full text of DOI:10.1021/jm01237a017

Products guided by the article

Product name:4-Chlor-2-nitro-1-<2-diaethylamino-aethoxy>-benzol

Cas No:95770-04-0

R&D Labs maybe for 95770-04-0

Suzhou SuKaiLu Chemical Technology Co., Ltd.

Contact:+86-512-62766020

Address:Floor 4, Building 1, Xinyi Pharmaceutical Valley Wisdom Industrial Park, 415 Changyang Street, Suzhou Industrial Park, Jiangsu Province
Ring Specialty Chemicals Inc.

website:http://www.ringchemicals.com/

Contact:+1-416-493-6870

Address:Toronto, Canada
Shanghai better-in Medical Technology Co.,LTD.

Contact:+86-21-38921049

Address:Lane 720 zhangjianggaoke cailun road, Pudong, Shanghai, room 513
BAODING SINO-CHEM INDUSTRY CO.,LTD

Contact:0312-5956088

Address:NO.8 FUXING ROAD,CHINA
Huayi Isotopes Co.

Contact:+ 86 512 52491118

Address:1 Fuyu Road, Haiyu TownChangshu, Jiangsu, China

Relevant to this article

Intramolecular Hetero-Diels-Alder Reaction of Alkylidene- and Benzylidenepyrazolones and Benzylideneisoxazolones. Investigations toward the Conformation of the Transition State

Doi:10.1021/jo00239a024
(1988)
Enantioselective mannich reactions with the practical proline mimetic N-(p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide

Doi:10.1021/jo8027938
(2009)
Direct Enzymatic Branch-End Extension of Glycocluster-Presented Glycans: An Effective Strategy for Programming Glycan Bioactivity

Doi:10.1002/chem.201604550
(2017)
α- and β-hydrazino acid-based pseudopeptides inhibit the chymotrypsin-like activity of the eukaryotic 20S proteasome

Doi:10.1016/j.ejmech.2013.09.059
(2013)
Regioselective Opening of Simple Epoxides with Diisopropylamine Trihydrofluoride

Doi:10.1021/jo00240a017
(1988)
Thiophene as a structural element of physiologically active compounds. 16. Thienoisoxazoles by substitution at the oxime nitrogen

Doi:10.1002/ardp.19873200911
(1987)

Article Doi

DOI: 10.1021/jm01237a017