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Methyl 5-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is a chemical compound with the molecular formula C13H16O3. It is a derivative of naphthalene and belongs to the class of carboxylate esters. Characterized by its aromatic structure and the presence of a methoxy group, Methyl 5-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is commonly used in the field of organic synthesis and pharmaceutical research. Its unique structure makes it a valuable precursor in the production of various pharmaceutical and agrochemical products. Additionally, due to its potential biological activity, it is also studied for its potential medicinal properties.

83781-71-9

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83781-71-9 Usage

Uses

Used in Organic Synthesis:
Methyl 5-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is used as a key intermediate in the synthesis of complex organic molecules. Its aromatic structure and methoxy group provide versatility in chemical reactions, making it a valuable building block for the development of new compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Methyl 5-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is used as a precursor for the production of various pharmaceutical products. Its unique structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Production:
Methyl 5-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is also utilized in the agrochemical industry for the development of new pesticides and other agricultural chemicals. Its chemical properties make it suitable for the synthesis of compounds with potential applications in crop protection and pest control.
Used in Medicinal Property Studies:
Due to its potential biological activity, Methyl 5-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is studied for its potential medicinal properties. Researchers are exploring its interactions with biological systems to identify possible therapeutic applications and develop new treatments for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 83781-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,8 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83781-71:
(7*8)+(6*3)+(5*7)+(4*8)+(3*1)+(2*7)+(1*1)=159
159 % 10 = 9
So 83781-71-9 is a valid CAS Registry Number.

83781-71-9SDS

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 Methyl 5-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 5-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate

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:83781-71-9 SDS

83781-71-9Downstream Products

83781-71-9Relevant academic research and scientific papers

Cycloaddition of o-quinodimethanes generated from 1,2-bis(bromomethyl)benzenes by constant-current electroreduction

Kise, Naoki,Mimura, Ryosuke,Ueda, Nasuo

, p. 2693 - 2694 (2002)

The constant-current electroreduction of 1,2-bis(bromomethyl)benzenes with dienophiles in NH4NO3-MeOH gave Diels-Alder cycloadducts in moderate-to-good yields.

Naphthalene derivatives as prostaglandin I2 agonsists

-

, (2008/06/13)

A compound of the formula STR1 wherein R1 is carboxy or protected carboxy, R2 is hydrogen, hydroxy or protected hydroxy, R3 is hydrogen, hydroxy, protected hydroxy, etc., R4 is hydrogen or halogen, A1

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