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5803-67-8

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5803-67-8 Usage

General Description

2-CHLORO-1-(5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHANONE is a chemical compound with the molecular formula C14H17ClO. It is a chlorinated ketone derivative with a substituted naphthalene ring structure. 2-CHLORO-1-(5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHANONE is used in various industrial applications, including as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a reagent in organic chemistry synthesis reactions. In addition, 2-CHLORO-1-(5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHANONE may have potential uses in the development of new materials and chemical compounds due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5803-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5803-67:
(6*5)+(5*8)+(4*0)+(3*3)+(2*6)+(1*7)=98
98 % 10 = 8
So 5803-67-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H13ClO/c13-8-12(14)11-6-5-9-3-1-2-4-10(9)7-11/h5-7H,1-4,8H2

5803-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-1-(5,6,7,8-tetrahydro-naphthalen-2-yl)-ethanone

1.2 Other means of identification

Product number -
Other names 2-chloro-1-(5,6,7,8-tetrahydronaphthalen-2-yl)ethanone

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:5803-67-8 SDS

5803-67-8Relevant articles and documents

N-(4-Substituted-thiazolyl)oxamic Acid Derivatives, a New Series of Potent, Orally Actve Antiallergy Agents

Hargrave, Karl D.,Hess, Friedrich K.,Oliver, James T.

, p. 1158 - 1163 (2007/10/02)

A series of N-(4-substituted-thiazolyl)oxamic acid derivatives were synthesized and tested for antiallergy activity in the rat PCA model.These compounds were conveniently prepared by treatment of the appropriate acetophenone with thiourea and iodine or by reaction of the chloroacetylbenzene with thiourea to give the corresponding aminothiazoles; subsequent condensation with ethyloxalyl chloride gave the thiazolyloxamates.Many of the analogues showed a 50percent inhibition at oxamic acid ethanolamine salt (61, PRH-836-EA), has been selected for further pharmacological evaluation.

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