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3-Ethoxycarbonyl-2-oxo-α-chromene-6-carboxylic acid is a heterocyclic chemical compound belonging to the class of chromene derivatives. It features a fused pyrone ring and a carboxylic acid moiety, which contribute to its potential pharmacological importance. 3-Ethoxycarbonyl-2-oxo-α-chromene-6-carboxylic acid has garnered interest due to its anti-inflammatory, anti-tumor, and antioxidant properties, making it a promising candidate for the development of new drugs to address various medical conditions. Its unique structure and properties render it a valuable asset in medicinal chemistry research and drug discovery endeavors.

6468-72-0

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6468-72-0 Usage

Uses

Used in Pharmaceutical Industry:
3-Ethoxycarbonyl-2-oxo-α-chromene-6-carboxylic acid serves as a key intermediate in the synthesis of pharmaceuticals, leveraging its anti-inflammatory properties for the treatment of conditions characterized by inflammation. Its potential to mitigate inflammation without causing significant side effects makes it an attractive option for drug development.
Used in Oncology Research:
In the field of oncology, 3-Ethoxycarbonyl-2-oxo-α-chromene-6-carboxylic acid is utilized as a compound with anti-tumor activity. Its capacity to target and inhibit the growth of cancer cells positions it as a candidate for further research and development into novel anticancer drugs, potentially offering new treatment options for patients with various types of cancer.
Used in Antioxidant Formulations:
3-Ethoxycarbonyl-2-oxo-α-chromene-6-carboxylic acid is employed as an antioxidant in the development of formulations aimed at combating oxidative stress. Its ability to neutralize free radicals and protect cells from damage makes it a valuable component in health supplements and therapeutic agents designed to promote overall health and well-being.
Used in Medicinal Chemistry Research:
3-Ethoxycarbonyl-2-oxo-α-chromene-6-carboxylic acid is also used as a research tool in medicinal chemistry, where its unique structure and properties are investigated for potential applications in drug discovery. Scientists explore its interactions with biological targets and evaluate its efficacy and safety in treating specific diseases, contributing to the advancement of medical knowledge and the creation of innovative treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 6468-72-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6468-72:
(6*6)+(5*4)+(4*6)+(3*8)+(2*7)+(1*2)=120
120 % 10 = 0
So 6468-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O6/c1-2-18-12(16)9-6-8-5-7(11(14)15)3-4-10(8)19-13(9)17/h3-6H,2H2,1H3,(H,14,15)

6468-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethoxycarbonyl-2-oxochromene-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-oxo-2H-chromene-3,6-dicarboxylic acid 3-ethyl ester

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:6468-72-0 SDS

6468-72-0Upstream product

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