Scholarly article on 2-Chloro-N-diethylcarbamoylmethyl-benzamide 37405-11-1 from Journal of Pharmaceutical Sciences p. 1331,1332

DOI: 10.1002/jps.2600610840

Source and publish data:

Journal of Pharmaceutical Sciences p. 1331,1332 (1972)

Update date:2022-08-05

Topics:

Authors:

Spencer Spencer

Doerge Doerge

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

Article abstract of DOI:10.1002/jps.2600610840

Full text of DOI:10.1002/jps.2600610840

Products guided by the article

Product name:2-Chloro-N-diethylcarbamoylmethyl-benzamide

Cas No:37405-11-1

R&D Labs maybe for 37405-11-1

VanderArk International Limited

Contact:86-10-82437576

Address:Qing He
Hangzhou LINGEBA Technology Co., Ltd.

Contact:+0086-571-87389059

Address:Office 1-913,NewYouth Plaza, GongShu Area, HangZhou,ZheJiang,P.R.China
Hangzhou J&H Chemical Co., Ltd.

website:http://www.jhechem.com/

Contact:+86-571-87396432

Address:No.200 Zhenhua Rd.Xihu Industrial Park, Hangzhou 310030, China
NINGBO PANGS CHEM INT’L CO., LTD.

Contact:+86-0574-27666801

Address:Floor 21, Building 11, Xintiandi, No. 689, Shijiroad, Ningbo, Zhejiang, China
Zhuhai Rundu Pharmaceutical co.,Ltd

Contact:+86-756-7630755

Address:No.6,North Airport Road,Sanzao Town,Jinwan District

Relevant to this article

3,4-Dialkoxypyrrole for the Formation of Bioinspired Rose Petal-like Substrates with High Water Adhesion

Doi:10.1021/acs.langmuir.6b02245
(2016)
Adenine derived inhibitors of the molecular chaperone HSP90 - SAR explained through multiple X-ray structures

Doi:10.1016/j.bmcl.2003.11.011
(2004)
Alkylation of chiral α-hydroxy ketones derived from (1R)-(+)-camphor. An asymmetric variant of the classical acetylene route to carbonyl compounds

Doi:10.1021/ol0163530
(2001)
Doi:10.1016/S0040-4039(01)84807-3
(1972)
Primary sulfonamide as a coupling partner: Copper(I)-catalyzed regioselective cross-coupling of 2-nitro benzenesulfonamides with thiol through the cleavage of Ar–SO₂NH₂ bonds

Doi:10.1080/00397911.2018.1441420
(2018)
Doi:10.1021/ja01131a051
(1952)

Article Doi

DOI: 10.1002/jps.2600610840