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Ethyl 8-methoxy-2-oxo-2H-chromene-3-carboxylate is a chemical compound with the molecular formula C13H12O5, belonging to the class of organic compounds known as 8-methoxy-2-oxo-2H-chromene-3-carboxylates. It is a chromene derivative that features a chromene moiety substituted at position 8 by a methoxy group and at position 2 by an oxo group. ethyl 8-methoxy-2-oxo-2H-chromene-3-carboxylate is recognized for its potential pharmacological properties, including anti-inflammatory and antitumor activities, making it a promising candidate in drug discovery and development.

1729-02-8

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1729-02-8 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 8-methoxy-2-oxo-2H-chromene-3-carboxylate is utilized as a building block for the synthesis of various bioactive compounds, contributing to the development of new pharmaceuticals with therapeutic potential.
Used in Drug Discovery and Development:
ethyl 8-methoxy-2-oxo-2H-chromene-3-carboxylate serves as an important intermediate in the synthesis of pharmaceuticals and agrochemicals, facilitating the creation of novel drugs with anti-inflammatory and antitumor properties, which are crucial for addressing various health conditions and diseases.
Used in Agrochemical Industry:
Ethyl 8-methoxy-2-oxo-2H-chromene-3-carboxylate is also employed in the agrochemical sector, where it plays a role in the synthesis of compounds that can be used for pest control and crop protection, thereby enhancing agricultural productivity and sustainability.

Check Digit Verification of cas no

The CAS Registry Mumber 1729-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1729-02:
(6*1)+(5*7)+(4*2)+(3*9)+(2*0)+(1*2)=78
78 % 10 = 8
So 1729-02-8 is a valid CAS Registry Number.

1729-02-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 8-methoxy-2-oxochromene-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-ethoxycarbonyl-8-methoxycoumarin

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:1729-02-8 SDS

1729-02-8Relevant academic research and scientific papers

Co-immobilization of Laccase and TEMPO in the Compartments of Mesoporous Silica for a Green and One-Pot Cascade Synthesis of Coumarins by Knoevenagel Condensation

Mogharabi-Manzari, Mehdi,Amini, Mohsen,Abdollahi, Mohammad,Khoobi, Mehdi,Bagherzadeh, Ghodsieh,Faramarzi, Mohammad Ali

, p. 1542 - 1546 (2018/02/28)

Co-immobilization of bio- and chemocatalysts produces sustainable, recyclable hybrid systems that open new horizons for green cascade approaches in organic synthesis. Here, the co-immobilization of laccase and 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) in mesoporous silica was used for the one-pot aqueous synthesis of 30 coumarin-3-carboxylate derivatives under mild conditions through the condensation of in situ oxidized 2-hydroxybenzyl alcohols and malonate derivatives. A maximum yield was obtained after incubating at pH 6.0 and 45 °C for 24 h. An efficient organic synthesis was catalyzed by the hybrid catalyst in 10 % organic solvent. More than 95 % of the initial activity of the enzyme was preserved after 10 cycles, and no significant catalyst deactivation occurred after 10 runs. This new system efficiently catalyzed the in situ aerobic oxidation of salicyl alcohols, followed by Knoevenagel condensation, which confirmed the possibility of producing efficient hybrid catalysts by co-immobilization of catalytic species in mesoporous materials.

Solvent-free coumarin synthesis

Sugino, Teizo,Tanaka, Koichi

, p. 110 - 111 (2007/10/03)

The synthesis of coumarins via Pechmann and Knoevenagel condensation reactions under solvent-free conditions is reported, in which waste minimization, simple operation and easier product work-up can be achieved.

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