Scholarly article on 3-Phenylcyclohexanone 2,4-dinitrophenyl hydrazone 25625-20-1 from Journal of the American Chemical Society p. 2174,2176

DOI: 10.1021/ja01186a054

Source and publish data:

Journal of the American Chemical Society p. 2174,2176 (1948)

Update date:2022-07-30

Topics:

Authors:

Woods Woods

Tucker Tucker

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

Article abstract of DOI:10.1021/ja01186a054

Full text of DOI:10.1021/ja01186a054

Products guided by the article

Product name:3-Phenylcyclohexanone 2,4-dinitrophenyl hydrazone

Cas No:25625-20-1

R&D Labs maybe for 25625-20-1

Jiaozuo Zhongwen Trading Coporation Limited

Contact:--

Address:East Renmin Road
SJZ Chenghui Chemical Co., Ltd.

Contact:86-311-87713916

Address:no.368 youyi north avenue
Evershine Chemical CO Ltd

Contact:+86-571-87010026

Address:202, Zhenhua Road,
WUXI HONOR SHINE CHEMICAL CO.,LTD

Contact:+86-510-83593312

Address:No.1699 Huishan avenue,Huishan district,Wuxi ,Jiangsu,China,214177.(Wuxi Huishan Ecomonic Develop Zone )
Hebei Kangtai Pharmaceutical Co.,Ltd

Contact:+86-0317-3512963

Address:Wugang Road,Mengcun of Cangzhou City,Hebei Province ,China

Relevant to this article

Optical sensing of cesium using 1,3-alternate calix[4]-mono- and di(anthrylmethyl)aza-crown-6

Doi:10.1111/j.1751-1097.1999.tb08297.x
(1999)
Synthesis and biological activity of a novel series of indole-derived PPARγ agonists

Doi:10.1016/S0960-894X(99)00603-4
(1999)
A concise synthesis of (-)-cytoxazone and its stereoisomers via imino 1,2-Wittig rearrangement

Doi:10.1055/s-1999-2992
(1999)
Reductive Arylation of Amides via a Nickel-Catalyzed Suzuki–Miyaura-Coupling and Transfer-Hydrogenation Cascade

Doi:10.1002/anie.202012048
(2021)
A versatile supported silver for heterogeneously catalysed processes: Synthesis of 3-Acyloxylindolines solvent-free conditions

Doi:10.1002/aoc.4130
(2018)
Conformationally rigid derivatives of WAY-267,464: Synthesis and pharmacology at the human oxytocin and vasopressin-1a receptors

Doi:10.1016/j.ejmech.2017.10.059
(2018)

Article Doi

DOI: 10.1021/ja01186a054