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154869-00-8

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154869-00-8 Usage

Molecular structure

2,3-Dimethoxy-11H-indeno[1,2-b]quinoline-10-carboxylic acid has a complex molecular structure, featuring a fused ring system of indeno[1,2-b]quinoline with two methoxy groups attached to the indene ring.

Chemical class

It belongs to the class of indenoquinoline carboxylic acids, which are derivatives of the parent compound indenoquinoline.

Methoxy groups

The compound contains two methoxy groups (-OCH3) attached to the indene ring, which can influence its chemical properties and reactivity.

Potential applications

This compound has potential applications in medicinal chemistry, particularly in the development of new drugs for the treatment of various diseases.

Promising candidate for research

Due to its unique structure and properties, 2,3-Dimethoxy-11H-indeno[1,2-b]quinoline-10-carboxylic acid is a promising candidate for further research in the fields of pharmacology and drug discovery.

Utility in chemical and biological studies

The compound's unique properties and structural features may also make it useful in various chemical and biological studies, contributing to a better understanding of its potential applications and interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 154869-00-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,8,6 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 154869-00:
(8*1)+(7*5)+(6*4)+(5*8)+(4*6)+(3*9)+(2*0)+(1*0)=158
158 % 10 = 8
So 154869-00-8 is a valid CAS Registry Number.

154869-00-8Downstream Products

154869-00-8Relevant articles and documents

Synthesis of substituted quinoline-4-carboxylic acids

Lackey,Sternbach

, p. 993 - 997 (2007/10/02)

A high yielding synthesis of a variety of quinoline-4-carboxylic acids has been accomplished using a modified Pfitzinger approach involving the condensation of a ketone with an isatin derivative employing aqueous acid conditions. A convenient synthesis of

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