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Methyl 6-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is a chemical compound with the molecular formula C12H14O3. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features a methyl ester group attached to the carboxylic acid functionality. The compound is characterized by a 1,2,3,4-tetrahydronapthalene core, which means that four hydrogen atoms have been added to the naphthalene ring, reducing its aromaticity. Additionally, it has a methoxy group (-OCH3) at the 6-position, which introduces an ether linkage and increases the molecule's polarity. Methyl 6-Methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features and reactivity.

2473-19-0

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2473-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2473-19-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2473-19:
(6*2)+(5*4)+(4*7)+(3*3)+(2*1)+(1*9)=80
80 % 10 = 0
So 2473-19-0 is a valid CAS Registry Number.

2473-19-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 1,2,3,4-tetrahydro-6-methoxynaphthalene-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

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More Details:2473-19-0 SDS

2473-19-0Relevant academic research and scientific papers

Palladium-catalyzed formal [4+2] cycloaddtion of o-xylylenes with olefins

Kuwano, Ryoichi,Shige, Takenori

, p. 3802 - 3803 (2008/02/03)

o-(Silylmethyl)benzylic carbonates reacted with various conjugated olefins in the presence of the palladium catalyst, which was generated in situ from Pd(η3-C3H5)Cp and 1,2-bis(diphenylphosphino)ethane (DPPE). The reaction

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