Scholarly article on 3-ethyl-3-amino-1-phenyl-hex-5-en-1-one 857545-66-5 from Journal of the American Chemical Society p. 2785,2788

DOI: 10.1021/ja01855a083

Source and publish data:

Journal of the American Chemical Society p. 2785,2788 (1941)

Update date:2022-08-03

Topics:

Authors:

Rehberg Rehberg

Henze Henze

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

Article abstract of DOI:10.1021/ja01855a083

Full text of DOI:10.1021/ja01855a083

Products guided by the article

Product name:3-ethyl-3-amino-1-phenyl-hex-5-en-1-one

Cas No:857545-66-5

R&D Labs maybe for 857545-66-5

Eastar Chemical Corporation

website:http://www.eastarchem.com/

Contact:1-800-898-2436

Address:1215 K Street, STE 1700
Guangzhou Shiny Co., Ltd.

website:https://www.sinoshiny.com/products

Contact:+86-20-62802632;62802633

Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District
SHIJIAZHUANG AGERUO-BIOTECH CO.LTD

Contact:+86-130-2866-6699

Address:Huaian east Road 158
Chinapeptides Co,. Ltd

Contact:+86-021-50792271

Address:Building 24A, 300 Chuantu Road, Chuansha, Pudong new area, Shanghai, China, 201202
SHANGHAI T&W PHARMACEUTICAL CO., LTD.

website:http://www.trustwe.com

Contact:+86-21-61551413

Address:601, No. 1, 2277 Nong, Zu Chongzhi Road, Zhangjiang Hightech. Park, Pudong

Relevant to this article

Doi:10.1021/jo01058a031
(1962)
SYNTHESIS OF 2,4-DIACETYL-6-C-β-D-GLUCOPYRANOSYLPHLOROGLUCINOL

Doi:10.1246/cl.1984.1039
(1984)
Potential antibacterial and antifungal activities of novel sulfamidophosphonate derivatives bearing the quinoline or quinolone moiety

Doi:10.1002/ardp.202000291
(2021)
The influence of steric effects on the kinetics and mechanism of S_NAr reactions of 1-phenoxy-nitrobenzenes with aliphatic primary amines in acetonitrile

Doi:10.1002/poc.3687
(2017)
A zig-zag [Mn^II₄] cluster from a novel bis(β-diketonate) ligand

Doi:10.1002/ejic.200600105
(2006)
Intermolecular chirality transfer from silicon to carbon: Interrogation of the two-silicon cycle for Pd-catalyzed hydrosilylation by stereoisotopochemical crossover

Doi:10.1021/ja067780h
(2007)

Article Doi

DOI: 10.1021/ja01855a083