Scholarly article on 2,2,2-trichloro-N-(4-phenylazo-phenyl)-acetamide 16112-66-6 from Journal of the American Chemical Society p. 2245,2248

DOI: 10.1021/ja01853a063

Source and publish data:

Journal of the American Chemical Society p. 2245,2248 (1941)

Update date:2022-08-03

Topics:

Authors:

Bergmann

Haskelberg

Bergmann

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

Article abstract of DOI:10.1021/ja01853a063

Full text of DOI:10.1021/ja01853a063

Products guided by the article

Product name:2,2,2-trichloro-N-(4-phenylazo-phenyl)-acetamide

Cas No:16112-66-6

R&D Labs maybe for 16112-66-6

Rudong Zhenfeng Yiyang Chemical Co., Ltd.

Contact:0513-84573047

Address:South Fengli Town, Rudong County, Jiangsu Province, China
Shanghai WinTide BioTechnology Co.,Ltd

Contact:86-21-37100630

Address:No. 908 Yunhe Road, Fengxian district, Shanghai
Chen jie

Contact:027-87677569

Address:Room 2203, yujingmingmen Buidling One, xiongchu Road, wuhan city, hubei province, China
Santow Laboratory Limited

Contact:+86-371-55981030

Address:Room 1571, Macalline Soho, No.1, Shangdu Road, Zhengzhou, Henan
Hangzhou Chemfar Ltd.

Contact:+86-571-87859231, 87859237, 87859239

Address:1606,Huarong Times Mansion, No.3880 Jiangnan Avenue, Binjiang District, Hangzhou, China, 310053

Relevant to this article

Chiral dienes as "ligands" for borane-catalyzed metal-free asymmetric hydrogenation of imines

Doi:10.1021/ja4025808
(2013)
Photochemically-mediated, nickel-catalyzed synthesis of N-(Hetero)aryl sulfamate esters

Doi:10.1021/acs.orglett.9b02621
(2019)
Stereochemical reassignment of heronamide A, a polyketide macrolactam from Streptomyces sp.

Doi:10.1016/j.tetlet.2013.01.012
(2013)
Development of 2′-substituted (2S,1′ R,2′S)-2- (carboxycyclopropyl)glycine analogues as potent N-methyl-d-aspartic acid receptor agonists

Doi:10.1021/jm400346a
(2013)
A simple and efficient synthesis of 3-amino-5-benzyl-6-phenylpyridazine-4- carbonitrile

Doi:10.1016/j.tetlet.2013.03.077
(2013)
Aminopyridine carbamic acid esters: Synthesis and potential as acetylcholinesterase inhibitors and acetylcholine releasers

Doi:10.1002/jps.2600810419
(1992)

Article Doi

DOI: 10.1021/ja01853a063