56820-58-7

Usage

Uses

Used in Pharmaceutical Production:
7-Chloro-1-hydroxynaphthalene is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs due to its unique chemical structure and reactivity.
Used in Dye Manufacturing:
In the dye industry, 7-Chloro-1-hydroxynaphthalene serves as a key component in the production of dyes, leveraging its chemical properties to create a range of colorants for different applications.
Used in Organic Chemical Synthesis:
7-Chloro-1-hydroxynaphthalene is employed as a building block in the synthesis of more complex organic molecules, playing a crucial role in advancing the field of organic chemistry and the creation of novel compounds with diverse properties.
Used in Research and Development:
7-Chloro-1-hydroxynaphthalene is used as a research compound in scientific studies, exploring its potential biological activities and applications in medicine, thereby contributing to the advancement of medical and scientific knowledge.
Used in Medical and Scientific Studies:
7-Chloro-1-hydroxynaphthalene is a subject of interest in medical and scientific research, where it is investigated for its potential biological activities, which may lead to new therapeutic approaches or insights into biological processes.

Upstream product

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• 90797-93-6 4-(4-chloro-phenyl)-but-3-enoic acid 
• 91058-94-5 6-chloro-4-hydroxy-2-naphthoic acid 
• 465-99-6 hedaragenin 
• 50987-58-1 7-chloronaphthalen-1-amine 
• 88-14-2 2-furanoic acid 
• 90500-14-4 5-chloro-2-iodosobenzoic acid 
• 117573-47-4 6-chloro-1,4-dihydro-1,4-epoxynaphthalene 
• 159268-93-6 7-chloro-1-acetoxynaphthalene 
• 91498-79-2 6-Chlor-4-methoxy-2-carboxy-naphthalin 
• 10026-13-8 phosphorus pentachloride 
• 89-77-0 2-Amino-4-chlorobenzoic acid 
• 13421-00-6 5-chloro-2-iodo-benzoic acid 
• 607-38-5 8-nitro-2-naphthylamine 

Downstream Products

• 2050-73-9 1,7-dichloronaphthalene 
• 25178-72-7 (7-chloro-[1]naphthyloxy)-acetic acid 
• 159268-94-7 4-phenyl-7-chloro-1,2,3,4-tetrahydronaphth-1-one 
• 159268-96-9 5-phenyl-8-chloro-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one 

Relevant academic research and scientific papers

Photocatalytic hydrogen evolution of 1-tetralones to α-naphthols by continuous-flow technology

Taking advantage of the synergy between photocatalysis and cobaloxime catalysis, the keto-enol radical cation of 1-tetralones becomes compatible with the transformation of various 1-tetralones into α-naphthols and H2 by virtue of the continuous-flow approach without any sacrificial oxidants under unusually mild conditions.

5-Phenyl-3-ureidobenzazepin-2-ones as cholecystokinin-B receptor antagonists

A series of 5-phenyl-3-ureidobenzazepin-2-one cholecystokinin-B (CCK-B) receptor antagonists was synthesized using Beckmann ring expansion of a suitable 4-phenyl-1-tetralone as a key step. Structure-activity relationship studies revealed the importance of

ARYNIC SPECIES; EFFECT OF SUBSTITUENTS ON THE REACTIVITY OF MONOSUBSTITUTED DEHYDROBENZENES

Evidence is presented demonstrating the existence of free dehydrobenzenes in the thermal decomposition of diaryliodonium-2-carboxylates, and that o-benzyne itself and its 4-methyl-, 4-chloro-, 4-bromo- and 4-nitro-derivatives are generated from insoluble polymer-bound precursors and trapped by a second solid phase in Diels-Alder reactions.Lifetimes for these elusive species are determined.

ARYNIC SPECIES II; TOSYL AND TRIAZENE AS LEAVING GROUP IN THE GENERATION OF ARYNES FROM POLYMER-BOUND REAGENTS

o-Benzyne and its 4-methyl, 4-chloro and 4-bromo-derivatives were generated in the thermal decomposition of two new kinds of polymer-bound precursors: 1(2-carboxyaryl)triazenes and 2-carboxyaryl-sulphonates.New kinds of trapping polymers for these elusive

GENERATION OF MONOSUBSTITUTED o-BENZYNES FROM POLYMERIC REAGENTS VIA HETEROLYTIC FRAGMENTATIONS

Generation of four 4-substituted o-benzynes by heterolytic fragmentation reactions is demonstrated.

2H-2-benzazepin-1,3-diones

A compound of the formula SPC1 Wherein X and R are as defined hereinafter, at least one of X and R being other than hydrogen, are provided and which are useful as central nervous system stimulants and for inducing increased motor activity as well as in vitro antimicrobial agents.