Scholarly article on 3,5-Dinitro-benzoic acid 2-ethoxycarbonyl-2-ethyl-cyclopentyl ester 38852-48-1 from Journal of the Chemical Society. Perkin transactions I p. 2776 - 2787

DOI: 10.1039/P19720002776

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 2776 - 2787 (1972)

Update date:2022-07-30

Topics:

Authors:

Gibson,K.H.

Saxton,J.E.

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

Article abstract of DOI:10.1039/P19720002776

Full text of DOI:10.1039/P19720002776

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

View Article Online

Products guided by the article

Product name:3,5-Dinitro-benzoic acid 2-ethoxycarbonyl-2-ethyl-cyclopentyl ester

Cas No:38852-48-1

R&D Labs maybe for 38852-48-1

Tianjin Jingye Fine Chemicals Co., Ltd.

Contact:+86-15722078107; +86-22-26911407

Address:Bohua Fine Chemicals Base of Petrochemical Industry Park, Nanhuan Road, Dagang District, Tianjin, 300271, P. R. China
TIANJIN FESTO CHEMICAL CO.,LTD(expird)

Contact:86-22-25814570

Address:No.12th,5th Ave.,TEDA,Tianjin,China
ShangHai Soyoung Biotechnology Inc

website:http://www.soyoungbio.com

Contact:+86-21-69893009

Address:shanghai
zhenjiang runjing high purity chemical co ltd

Contact:+86-511-83361155

Address:No.8.haixi road,international chemical park
CHEMINN LTD.

website:http://www.cheminn.com/

Contact:86-531-67875205

Address:No.9-2,South of Shanda Road, Jinan ,China

Relevant to this article

Novel route to azobenzenes via Pd-catalyzed coupling reactions of aryl hydrazides with aryl halides, followed by direct oxidations

Doi:10.1021/ol027311u
(2003)
248. Methylation reactions of 30-oxa-(14)-cytochalasanes

Doi:10.1002/hlca.19720550725
(1972)
Doi:10.1055/s-1970-21634
(1970)
Doi:10.1139/v72-513
(1972)
The synthesis of substituted 2-aminophenyl heterocycic ketones

Doi:10.1080/00397919308013295
(1993)
Co(II)/Cu(II)-cocatalyzed oxidative C-H/N-H functionalization of benzamides with ketones: A facile route to isoindolin-1-ones

Doi:10.1039/c9cc02661d
(2019)

Article Doi

DOI: 10.1039/P19720002776

Source and publish data: