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2-Phenylimidazole-4,5-dicarboxylic acid is a chemical compound with the molecular formula C11H7NO4. It is a derivative of imidazole, a heterocyclic aromatic organic compound, featuring a phenyl group attached to the imidazole ring at the 2-position. The compound has two carboxylic acid functional groups at the 4 and 5 positions, which contribute to its acidic properties. This organic molecule is known for its potential applications in pharmaceuticals and materials science, particularly in the synthesis of various bioactive compounds and as a building block for more complex molecules. Its chemical structure and properties make it a versatile intermediate in organic synthesis, with potential uses in the development of new drugs and other chemical products.

3137-17-5

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3137-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3137-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3137-17:
(6*3)+(5*1)+(4*3)+(3*7)+(2*1)+(1*7)=65
65 % 10 = 5
So 3137-17-5 is a valid CAS Registry Number.

3137-17-5Relevant academic research and scientific papers

Synthesis and antiproliferative activity of imidazole and imidazoline analogs for melanoma

Chen, Jianjun,Wang, Zhao,Lu, Yan,Dalton, James T.,Miller, Duane D.,Li, Wei

body text, p. 3183 - 3187 (2009/04/11)

We have previously reported substituted 2-aryl-thiazolidine-4-carboxylic acid amides as potent and selective antiproliferative agents for melanoma. To understand the importance of the thiazolidine ring and to reduce potential complications associated with the two chiral centers, we designed and synthesized sets of new analogs by modifying this ring. These new analogs were tested in two melanoma cell lines and fibroblast cells (negative controls). Compared with the older analogs containing the thiazolidine ring, these new analogs have lower potency in general, but some of these analogs still have very good selectivity. These structure-activity studies indicated that the thiazolidine ring is very critical for the activity for these series of compounds.

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