6742-26-3 Usage
Description
Ethyl 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate is an organic ester compound characterized by its complex structure, which includes an ethyl group, a carboxylic acid group, and a naphthalene ring. This versatile molecule is recognized for its potential as a building block in the synthesis of pharmaceuticals and agrochemicals, as well as for its applications in the food and beverage industry as a fragrance ingredient and flavoring agent.
Uses
Used in Pharmaceutical and Agrochemical Industries:
Ethyl 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate serves as a valuable precursor in organic chemistry, utilized in the synthesis of a variety of pharmaceuticals and agrochemicals. Its unique structure and functional groups enable the creation of diverse molecules with distinct biological and chemical properties, contributing to the development of new and effective compounds for these industries.
Used in Food and Beverage Industry:
In the food and beverage sector, ethyl 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate is employed as a fragrance ingredient and flavoring agent. Its aromatic properties allow it to enhance the sensory experience of various products, adding depth and complexity to their scents and tastes.
Safety Considerations:
It is crucial to handle and use ethyl 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate with caution, as it may present potential health and safety risks if not properly managed. Adequate measures should be taken to mitigate any hazards associated with its use, ensuring the well-being of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6742-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6742-26:
(6*6)+(5*7)+(4*4)+(3*2)+(2*2)+(1*6)=103
103 % 10 = 3
So 6742-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H14O3/c1-2-16-13(15)11-8-7-9-5-3-4-6-10(9)12(11)14/h3-6,11H,2,7-8H2,1H3/t11-/m1/s1
6742-26-3Relevant articles and documents
Construction of Polycyclic β-Ketoesters Using a Homoconjugate Addition/Decarboxylative Dieckmann Annulation Strategy
Chen, Zhiwei,Hong, Allen Y.,Linghu, Xin
, p. 6225 - 6234 (2018/05/29)
The construction of arene-fused cyclic β-ketoesters from 2-iodoaryl esters and 1,1-cyclopropane diesters is detailed. The synthetic method takes advantage of a CuI·SMe2-mediated homoconjugate addition followed by a decarboxylative Dieckmann cyclization to afford valuable polycyclic building blocks. Various iodoaryl esters and 1,1-cyclopropane diesters were evaluated, and the limitations of both reactions are discussed. Several mechanistic probes are detailed and synthetic applications are described.
