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6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester is a complex chemical compound that is a methyl ester derivative of 6-methoxy-4-oxo-1,4-dihydroquinoline-2-carboxylic acid, belonging to the quinoline class of compounds. It features a quinoline core with a methoxy group at the 6-position and a carboxylic acid group at the 2-position, which is esterified with a methyl group. 6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester has potential applications in pharmaceutical research due to its unique structure and possible biological activity, although its specific properties and uses are not extensively documented.

82633-20-3

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82633-20-3 Usage

Uses

Used in Pharmaceutical Research:
6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester is used as a research compound for exploring its potential biological activity and therapeutic applications. Its quinoline core may confer certain pharmacological properties, making it a candidate for further investigation in drug development.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester is used as a starting material or intermediate for the synthesis of more complex molecules with potential therapeutic effects. Its unique structural features can be exploited to design and develop new drugs targeting specific biological pathways or receptors.
Used in Drug Discovery:
6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester is utilized in drug discovery processes to identify novel lead compounds with potential therapeutic benefits. Its chemical properties and interactions with biological targets can be studied to optimize its pharmacological profile and selectivity.
Used in Chemical Synthesis:
6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester serves as a versatile building block in organic synthesis, allowing for the preparation of a variety of quinoline-based derivatives with diverse applications in chemistry and related fields.
Safety Precautions:
As with any chemical compound, special care should be taken when handling and using 6-Methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester to minimize potential health and safety hazards. Proper protective equipment, such as gloves and eyewear, should be worn, and the compound should be stored and disposed of according to established safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 82633-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,3 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82633-20:
(7*8)+(6*2)+(5*6)+(4*3)+(3*3)+(2*2)+(1*0)=123
123 % 10 = 3
So 82633-20-3 is a valid CAS Registry Number.

82633-20-3SDS

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-4-oxo-1H-quinoline-2-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 6-methoxy-4-oxo-1,4-dihydroquinoline-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82633-20-3 SDS

82633-20-3Upstream product

82633-20-3Downstream Products

82633-20-3Relevant academic research and scientific papers

2-AMINOCARBONYL-QUINOLINE COMPOUNDS AS PLATELET ADENOSINE DIPHOSPHATE RECEPTOR ANTAGONISTS

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Page 43, (2010/02/07)

Compounds of formula (I), where m, n, R1, R2, R3, R4 and R6 are described herein, are useful as inhibitors of platelet adenosine diphosphate. Pharmaceutical compositions containing these compounds, methods of using these compounds as antithrombotic agents and processes for synthesizing these compounds are also described herein.

Platelet adenosine diphosphate receptor antagonists

-

, (2008/06/13)

Compounds of the following formula (I): where a, b, R1, R2, R4 and R6 are described herein, are useful as inhibitors of platelet adenosine diphosphate. Pharmaceutical compositions containing these compounds, met

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