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2-Naphthalenethiol is an organosulfur compound with the formula C 10 H 7 SH. It is a white solid. It is a white solid. It is one of two mono thiols of naphthalene , the other being 1-naphthalenethiol .
2-Naphthalenethiol This page was last edited on 13 November 2022, at 22:54 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
2-Naphthol, or β-naphthol, is a fluorescent colorless (or occasionally yellow) crystalline solid with the formula C 10 H 7 OH. It is an isomer of 1-naphthol, differing by the location of the hydroxyl group on the naphthalene ring.
[1] 1-Naphthalenethiol can also be prepared from 1-bromonaphthalene by Pd-catalyzed reaction with the silylthiolate i Pr 3 SiSK followed by hydrolysis of the silathioether. [2] It was first prepared from the Grignard reagent generated from 1-bromonaphthalene. Treatment of that reagent with elemental sulfur followed by acidification gave the ...
This page was last edited on 8 November 2022, at 18:36 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
2-Naphthoic acid is an organic compound of the formula C 10 H 7 CO 2 H. It is one of two isomeric carboxylic acid derivatives of naphthalene , the other one being 1-naphthoic acid . It can be prepared by carboxylation of 1-chloronaphthalene .
This page was last edited on 8 November 2022, at 19:45 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
2-Naphthylamine or 2-aminonaphthalene is one of two isomeric aminonaphthalenes, compounds with the formula C 10 H 7 NH 2. It is a colorless solid, but samples take on a reddish color in air because of oxidation. It was formerly used to make azo dyes, but it is a known carcinogen and has largely been replaced by less toxic compounds. [2]