Scholarly article on phenylacetic acid N'-benzoyl-N-phenyl-hydrazide 27389-34-0 from Journal of the Chemical Society C: Organic p. 1397 - 1401

DOI: 10.1039/j39700001397

Source and publish data:

Journal of the Chemical Society C: Organic p. 1397 - 1401 (1970)

Update date:2022-08-05

Topics:

Authors:

Boyd,G.V.

Dando,S.R.

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

Article abstract of DOI:10.1039/j39700001397

Full text of DOI:10.1039/j39700001397

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:phenylacetic acid N'-benzoyl-N-phenyl-hydrazide

Cas No:27389-34-0

R&D Labs maybe for 27389-34-0

puyang hongda shengdao new material co.,ltd.

Contact:+86-393- 4896278

Address:No.29 East Zhongyuan Road
taicang liyuan chemical co,.ltd

website:http://www.tcliyuanchem.com/productse.php

Contact:86-512-53539583

Address:Room 804,Huaxu Building,No.95,Renmin South Road,Taicang city,Jiangsu Province,China
HANGZHOU YUNUO CHEMICAL CO.,LTD

website:http://www.yunuochem.com

Contact:0571-83715115

Address:hangzhou
X.T.Y Environ-Tech Co.,Ltd

Contact:+86-310-7092106

Address:Quzhou Modern & New Industrial Park, Handan, Hebei 057250, China
Changyi Xinxing Technology Development Co., Ltd.

Contact:0086-510-86651065(Time Zone:8),86651656

Address:94 Yingbinxilu WestRoad, Huangtu Town, Jiangyin City, Jiangsu, China

Relevant to this article

A chromium-free synthesis of enantiopure 5-oxoborneol

Doi:10.1016/j.tetlet.2011.06.076
(2011)
Synthesis, structure, photoluminescence and photoreactivity of 2,3-diphenyl-4-neopentyl-l-silacyclobut-2-enes

Doi:10.1002/chem.200901323
(2009)
Redox-Neutral Access to Isoquinolinones via Rhodium(III)-Catalyzed Annulations of O-Pivaloyl Oximes with Ketenes

Doi:10.1021/acs.orglett.8b00906
(2018)
Direct Observation of an Imidoylnitrene: Photochemical Formation of PhC(=NMe)?N and Me?N from 1-Methyl-5-phenyltetrazole

Doi:10.1002/anie.201712689
()
Rapid assembly of α-ketoamides through a decarboxylative strategy of isocyanates with α-oxocarboxylic acids under mild conditions

Doi:10.1039/d1ob00562f
(2021)
Doi:10.1021/ja01248a026
(1943)

Article Doi

DOI: 10.1039/j39700001397