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5-Chloro-8-methoxyl-2-tetralone is a chemical compound with the formula C11H9ClO2, belonging to the tetralone derivatives. It features a chlorine atom at the 5th position and a methoxy group at the 8th position, which endows it with unique chemical properties and potential applications in various fields.

136949-71-8

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136949-71-8 Usage

Uses

Used in Pharmaceutical Applications:
5-Chloro-8-methoxyl-2-tetralone is used as a potential anti-inflammatory and antioxidant agent due to its ability to modulate biological processes associated with inflammation and oxidative stress. Its chemical structure allows it to interact with specific targets in the body, offering therapeutic benefits in treating conditions characterized by inflammation and oxidative damage.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-Chloro-8-methoxyl-2-tetralone is used as a substrate for various chemical reactions. Its unique functional groups and structural features make it an interesting candidate for the synthesis of new compounds with potential therapeutic properties. Researchers utilize 5-Chloro-8-methoxyl-2-tetralone to explore novel synthetic pathways and develop innovative drug candidates.
Used in Organic Chemistry Research:
5-Chloro-8-methoxyl-2-tetralone is also of interest to researchers in the field of organic chemistry. Its reactivity and the presence of specific functional groups make it a valuable tool for studying reaction mechanisms, exploring new synthetic methods, and understanding the fundamental principles of organic reactions. 5-Chloro-8-methoxyl-2-tetralone contributes to the advancement of organic chemistry by providing insights into the behavior of similar molecules and their potential applications.
Overall, 5-Chloro-8-methoxyl-2-tetralone has demonstrated its potential in various applications, particularly in the pharmaceutical and chemical research fields. Its unique chemical properties and versatility in chemical reactions make it a promising compound for further study and development in the creation of new drugs and other applications.

Check Digit Verification of cas no

The CAS Registry Mumber 136949-71-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,4 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136949-71:
(8*1)+(7*3)+(6*6)+(5*9)+(4*4)+(3*9)+(2*7)+(1*1)=168
168 % 10 = 8
So 136949-71-8 is a valid CAS Registry Number.

136949-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-8-methoxy-3,4-dihydro-1H-naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 5-chloro-8-methoxyl-2-tetralone

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:136949-71-8 SDS

136949-71-8Upstream product

136949-71-8Relevant academic research and scientific papers

Design, synthesis, and structure-activity relationships of a new series of α-adrenergic agonists: Spiro[(1,3-diazacyclopent-1-ene)-5,2'-(1',2',3',4'- tetrahydronaphthalene)]

Cordi,Lacoste,Descombes,Courchay,Vanhoutte,Laubie,Verbeuren

, p. 4056 - 4069 (2007/10/03)

The contractions induced by a partial α1-adrenoceptor agonist in cutaneous veins, such as the saphenous vein, show a particular sensitivity to changes in local temperature: the contractility to a partial α1- adrenoceptor agonist incr

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