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56820-58-7

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56820-58-7 Usage

General Description

7-Chloro-1-hydroxynaphthalene is a chemical compound with the molecular formula C10H7ClO. It is a derivative of naphthalene that contains a chlorine atom and a hydroxyl group attached to the aromatic ring. 7-Chloro-1-hydroxynaphthalene is used in the production of pharmaceuticals, dyes, and other organic chemicals. It is also employed in research and development as a building block for the synthesis of more complex molecules. Additionally, 7-Chloro-1-hydroxynaphthalene has been investigated for its potential biological activities and is a subject of interest in medical and scientific studies.

Check Digit Verification of cas no

The CAS Registry Mumber 56820-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,2 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56820-58:
(7*5)+(6*6)+(5*8)+(4*2)+(3*0)+(2*5)+(1*8)=137
137 % 10 = 7
So 56820-58-7 is a valid CAS Registry Number.

56820-58-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloronaphthalen-1-ol

1.2 Other means of identification

Product number -
Other names 1-Naphthalenol, 7-chloro-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56820-58-7 SDS

56820-58-7Relevant articles and documents

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Winterstein,Maxim

, p. 202 (1919)

-

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

Lowe III,Hageman,Drozda,McLean,Bryce,Crawford,Zorn,Morrone,Bordner

, p. 3789 - 3811 (2007/10/02)

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

Gavina, F.,Luis, S. V.,Costero, A. M.

, p. 155 - 166 (2007/10/02)

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.

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