Autoxidation of 3-Hydroxyanthranilic Acid

DOI: 10.1021/jo00242a026

Source and publish data:

Journal of Organic Chemistry p. 1486 - 1488 (1988)

Update date:2022-09-26

Topics: Kinetics Autoxidation Spectroscopy Free radicals 3-Hydroxyanthranilic acid

Authors:

Manthey, Michael K.

Pyne, Stephen G.

Truscott, Roger J. W.

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

Article abstract of DOI:10.1021/jo00242a026

3-Hydroxyanthranilic acid in aqueous solution can be autoxidized to yield two different products depending on the pH at which the oxidation is performed.At acidic pH the formation of cinnabarinic acid is favored while at alkaline pHs the major product is

Full text of DOI:10.1021/jo00242a026

Products guided by the article

Product name:1,4-Cyclohexadiene-1-carboxylic acid, 2-amino-3,6-dioxo-5-[(phenylmethyl)amino]-, monosodium salt

Cas No:112817-52-4

R&D Labs maybe for 112817-52-4

Zhejiang kehong chemical co., ltd

Contact:0086-575-85522000

Address:xiner center RD binhai industrial zone shaoxing zhejiang province P.R.China,312073
Xi'an HO-SHINE Bio-Technology Co., Ltd

Contact:+86 (29) 8248-5435/18292020086

Address:No.6 Shiyuan Road Xian City Shaanxi Province, 710048 China
Shanghai Balmxy Pharmaceutical Co., Ltd

Contact:0086-21-24206007

Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China
Huzhou City Linghu Xinwang Chemical Co.,Ltd.

Contact:86-572-3948695/3945236

Address:huzhou
Xinchang Yueding Chemical Co., Ltd.

Contact:86-571-56926323

Address:NO.90 BEIMENCHENGWAI CHENGGUAN TOWN XINCHANG

Relevant to this article

Isolation and Structure of Magnoloside A, a New Phenylpropanoid Glycoside from Magnolia obovata Thunb.

Doi:10.1246/cl.1988.163
(1988)
External Oxidant-Free Oxidative Tandem Cyclization: NaI-Catalyzed Thiolation for the Synthesis of 3-Thiosubstituted Pyrroles

Doi:10.1002/adsc.201900620
(2019)
Syntheses, characterizations and theoretical calculations of rhodium(III) 1,2-naphthoquinone-1-oxime complexes

Doi:10.1016/j.ica.2009.12.033
(2010)
A thermally-induced, tandem [3,3]-sigmatropic rearrangement/[2 + 2] cycloaddition approach to carbocyclic spirooxindoles

Doi:10.3762/bjoc.6.33
(2010)
Cyclopropylmethyl Protection of Phenols: Total Synthesis of the Resveratrol Dimers Anigopreissin A and Resveratrol–Piceatannol Hybrid

Doi:10.1002/open.201800214
(2018)
Fused tetrazoles as azide surrogates in click reaction: Efficient synthesis of N-heterocycle-substituted 1,2,3-triazoles

Doi:10.1021/ol100745d
(2010)

Article Doi