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2-(2,3-Dihydro-1H-inden-5-ylcarbonyl)benzene carboxylic acid is a complex organic compound with the chemical formula C17H14O3. It is a derivative of benzoic acid, featuring a 2,3-dihydro-1H-inden-5-ylcarbonyl group attached to the 2-position of the benzene ring. This molecule is characterized by its aromatic structure and the presence of a carbonyl group, which contributes to its reactivity and potential applications in various chemical processes. The compound may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and functional groups.

6321-58-0

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6321-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6321-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6321-58:
(6*6)+(5*3)+(4*2)+(3*1)+(2*5)+(1*8)=80
80 % 10 = 0
So 6321-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H14O3/c18-16(14-6-1-2-7-15(14)17(19)20)13-9-8-11-4-3-5-12(11)10-13/h1-2,6-10H,3-5H2,(H,19,20)

6321-58-0Relevant academic research and scientific papers

Synthesis and Biological Evaluation of New Phthalazinone Derivatives as Anti-Inflammatory and Anti-Proliferative Agents

Hameed, Alhamzah Dh.,Ovais, Syed,Yaseen, Raed,Rathore, Pooja,Samim, Mohammed,Singh, Surender,Sharma, Kalicharan,Akhtar, Mymona,Javed, Kalim

, p. 150 - 159 (2016/02/09)

The chemistry of phthalazine derivatives has been of increasing interest since many of these compounds have found many chemotherapeutic applications. So this study aims to synthesize a library of phthalazine derivatives and to investigate their anti-inflammatory and anti-proliferative activities. Sixteen new phthalazinone derivatives (2a-p) were synthesized and tested for their in vitro antiproliferative and in vivo anti-inflammatory activities. All the synthesized compounds were identified and characterized by IR, 1H NMR, 13C NMR spectroscopy, and MS. Two compounds, 2b and 2i, showed significant anti-inflammatory activity comparable with that of the standard drug etoricoxib in the carrageenan-induced rat paw edema model at 3 and 5 h, respectively. Three compounds (2h, 2j, and 2g) showed moderate sensitivity toward the renal cancer cell line UO-31. A library of new phthalazone compounds (2a-p) was synthesized as dual inhibitors (COX-2/LOX-5) and evaluated for their anti-inflammatory, anticancer activities. Two compounds showed significant anti-inflammatory activity comparable with that of the standard drug etoricoxib, whereas three compounds showed moderate sensitivity toward the renal cancer cell line UO-31.

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