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

Wuhan Soleado Technology Co.,Ltd.

Contact:86-2783341481 18971291927

Address:RM2405 Unit 1 Builing 1, Taiyin Tower, Changqing Road,Wuhan China
Langchem

Contact:+86+21-58956006 15800617331

Address:402 Room, 150# Cailun Road, Zhangjiang high tech park, Shanghai
TAIXING BEST NEW MATERIALS CO., LTD

Contact:0523-87998158;

Address:No.18 Zhonggang Road，Taixing City ，Jiangsu , China
Jiangxi Hito Chemical Co., Ltd.

Contact:+86-792-3170318

Address:No. 6, Tianhong Ave., Xinghuo Industry Park, Yongxiu, Jiujiang, Jiangxi, China
Water Chemical Co.,LTD

Contact:+86-21-6856-1349 523-87676172

Address:No16 . BinJiang Road . Taixing Economy Developing Area .JiangSu Province . China

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