Preparation of Naphthalene-2,3,6,7-tetracarboxylic Acid

DOI: 10.1246/cl.1988.1933

Source and publish data:

Chemistry Letters p. 1933 - 1936 (1988)

Update date:2022-08-03

Topics:

Authors:

Chiba, Koji

Tagaya, Hideyuki

Kono, Hiroshi

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

Article abstract of DOI:10.1246/cl.1988.1933

In the presence of sodium iodide and cadmium oxide, sodium 1-naphthoate was effectively converted into naphthalene-2,3,6,7-tetracarboxylate at 480 deg C under carbon dioxide pressure.The minor product was naphthalene-2,6-dicarboxylate.Also in the rearrangement of sodium 2-naphthoate, the addition effect of sodium iodide was observed.

Full text of DOI:10.1246/cl.1988.1933

Products guided by the article

Product name:naphthalene-2,3-dicarboxylic acid

Cas No:17273-36-8

R&D Labs maybe for 17273-36-8

Lonzeal Pharmaceuticals Co., Ltd.

website:http://www.lonzeal.com

Contact:+86-13381011962

Address:RM 801, Yue MOMA, No. 26 Anningzhuang Rd. Haidian District, Beijing, China
Tianjin SPHINX SCIENTIFIC LAB.

Contact:+86-022-66211289

Address:Tianda high-tech Park. No.80,the 4th Avenue
shanghai jinshan pharmaceutical Co.,Ltd

Contact:021-57363011，13681638167

Address:No. 7966 Tingfeng Road,Jinshan,Shanghai,China
Huayi Isotopes Co.

Contact:+ 86 512 52491118

Address:1 Fuyu Road, Haiyu TownChangshu, Jiangsu, China
Yangzhou Zhongbao Pharmaceutical Co.,Ltd

Contact:+86-514-88290838

Address:Jiangsu Baoying county economic develpment zone in baoying avenue91

Relevant to this article

Structure-activity relationships (SAR) of [D-Arg(2)]dermorphin(1-4) analogues, N(alpha)-amidino-Tyr-D-Arg-Phe-X.

Doi:10.1248/cpb.50.771
(2002)
Alkynylhalocarbenes 3. * Synthesis of 2-(alk-1-ynyl)oxiranes from 1,1-dichloroalk-2-ynes and 3-substituted 3-bromo-1,1,1-trichloropropanes under the action of potassium tert-butoxide in the presence of alkali metal alkoxides

Doi:10.1007/bf02503489
(1998)
Unusual reactivity of (vinylimino)phosphoranes and their utility in the preparation of pyridine and dihydropyridine derivatives

Doi:10.1021/jo960940v
(1996)
The umpolung of substituent effect in nucleophilic aromatic substitution. A new approach to the synthesis of N,N-disubstituted melamines (triazine triskelions) under mild reaction conditions

Doi:10.1016/j.tet.2009.03.017
(2009)
Synthesis and Biological Activity of some new Pyridazine Derivatives

Doi:10.1007/BF00824306
(1995)
Identification of N-arylsulfonylpyrimidones as anticancer agents

Doi:10.1007/s12272-018-1003-9
(2018)

Article Doi