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2-Ethoxycarbonyl-3-coumaranone, also known as ethyl 3-coumaranone-2-carboxylate, is a chemical compound with the molecular formula C12H12O4. It is a derivative of coumarin, a natural substance found in many plants and used in perfumes and flavorings. 2-ETHOXYCARBONYL-3-COUMARANONE is known for its antimicrobial, antioxidant, and anti-inflammatory properties, making it a versatile substance with potential applications in various industries.

13099-95-1

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13099-95-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Ethoxycarbonyl-3-coumaranone is used as a synthetic intermediate for the production of various pharmaceuticals. Its antimicrobial, antioxidant, and anti-inflammatory properties contribute to the development of new drugs that can address a range of health issues.
Used in Fragrance Industry:
In the fragrance industry, 2-Ethoxycarbonyl-3-coumaranone is used as a component in creating unique scents. Its natural origin and compatibility with other fragrance compounds make it a valuable addition to perfumes and other scented products.
Used in Food Preservation:
2-Ethoxycarbonyl-3-coumaranone is studied for its potential use in food preservation due to its antimicrobial activity against foodborne pathogens. This property can help extend the shelf life of food products and improve food safety.
Used in Antimicrobial Applications:
2-Ethoxycarbonyl-3-coumaranone is used as an antimicrobial agent in various applications, including medical, industrial, and consumer products. Its ability to inhibit the growth of bacteria and other microorganisms makes it a promising candidate for use in sanitizing and disinfecting solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 13099-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,9 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13099-95:
(7*1)+(6*3)+(5*0)+(4*9)+(3*9)+(2*9)+(1*5)=111
111 % 10 = 1
So 13099-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O4/c1-2-14-11(13)10-9(12)7-5-3-4-6-8(7)15-10/h3-6,10H,2H2,1H3

13099-95-1SDS

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 Ethyl 3-oxo-2,3-dihydrobenzofuran-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Ethoxycarbonyl-3-coumaranone

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:13099-95-1 SDS

13099-95-1Relevant academic research and scientific papers

Synthesis and biological evaluaton of N'-(4- substitutedbenzylidene)-3'-methoxybenzofuran-2'-carbohydrazide derivatives as potential anticancer agents

Sharma, Gyanendra Kumar,Sain, Ashok,Pathak, Devender

, p. 353 - 358 (2019/01/21)

In the present study we have made an attempt to synthesize novel benzofuran derivatives and evaluate them for anticancer screening. First, 2-carbethoxy-3 (2H) benzofuranone (2) was prepared by the condensation of ethyl bromomalonate with methyl salicylate

Diastereo- and enantioselective propargylation of benzofuranones catalyzed by pybox-copper complex

Zhao, Long,Huang, Guanxin,Guo, Beibei,Xu, Lijun,Chen, Jie,Cao, Weiguo,Zhao, Gang,Wu, Xiaoyu

supporting information, p. 5584 - 5587 (2015/02/19)

Diastereo- and enantioselective preparation of 2,2-disubstituted benzofuran-3(2H)-one has been realized by a pybox-copper catalyzed reaction between 2-substituted benzofuran-3(2H)-one and propargyl acetate. The utility of this method was demonstrated by further transformation of the terminal alkyne into a methyl ketone without loss of enantiomeric purity.

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