Scholarly article on (2-diethylamino-ethyl)-phenyl-malonic acid diethyl ester 58790-89-9 from Journal of the American Chemical Society p. 448,451

DOI: 10.1021/ja01145a143

Source and publish data:

Journal of the American Chemical Society p. 448,451 (1951)

Update date:2022-08-04

Topics:

Authors:

McElvain

Laughton

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

Article abstract of DOI:10.1021/ja01145a143

Full text of DOI:10.1021/ja01145a143

Products guided by the article

Product name:(2-diethylamino-ethyl)-phenyl-malonic acid diethyl ester

Cas No:58790-89-9

R&D Labs maybe for 58790-89-9

Tianjin Jiuri New Materials Co., Ltd.

Contact:+86-22-58889220

Address:C-5/6, Vison Hill, No.1 Gonghua Road, Huayuan Hi-tech Park, Tianjin, China.
Changsha Huajing Powdery Material Technological Co., Ltd.

Contact:86-731-88879686

Address:Building 2, West Garden, Main Campus of Central South University, Changsha, Hunan Province, China
Wuhan HengHeDa Pharm Co., Ltd

Contact:86-27-84888681

Address:Wuhan economic & technology development zone
Shanghai PengMo Biotechnology Co.,Ltd

website:http://www.pengmobio.lookchem.com

Contact:86-13052359378

Address:No.218 Hai Qu Road.Shanghai.China
Beijing Tianjia Chemical Science & Technology Co.,Ltd

Contact:86-0550-2392698

Address:No.388, Shiliang Road (East),

Relevant to this article

Synthesis, biological activity evaluation and molecular modeling study on the new isoconessimine derivatives as acetylcholinesterase inhibitors

Doi:10.1002/cjoc.201300441
(2013)
Reaction of 4-Alkylaminodihydro-2(1H)-pyridinethions and -ones resp. with Bis-trichlorophenyl-ethylmalonate

Doi:10.1007/BF00800264
(1982)
The mitomycin antibiotics. Synthetic studies. XX. N-substituted carbamoyl and acyl esters of a related 3-hydroxymethyl-4,7-indoloquinone.

Doi:10.1021/jm00310a041
(1968)
Doi:10.1246/bcsj.49.224
(1976)
D-Phe-Pro-Arg type thrombin inhibitors: Unexpected selectivity by modification of the P1 moiety

Doi:10.1016/S0960-894X(03)00347-0
(2003)
Structural Characterization of Thiocyclophanes That Promote Edge-to-Face Aromatic-Aromatic Geometries

Doi:10.1021/jo00118a030
(1995)

Article Doi

DOI: 10.1021/ja01145a143

Source and publish data: