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1,5-bis-(4-chloro-phenyl)-pentane-1,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35333-17-6

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35333-17-6 Usage

General Description

1,5-bis-(4-chloro-phenyl)-pentane-1,5-dione, also known as diclofenac, is a pharmaceutical compound belonging to the class of non-steroidal anti-inflammatory drugs (NSAIDs). It is commonly used to reduce pain and inflammation in conditions such as arthritis, gout, and migraine. Diclofenac works by inhibiting the production of inflammatory molecules called prostaglandins, which are responsible for pain and swelling. Its chemical structure consists of two aromatic rings with chlorine substituents attached to a pentane-1,5-dione backbone. 1,5-bis-(4-chloro-phenyl)-pentane-1,5-dione is typically administered orally or topically and is available in various forms such as tablets, gels, and patches. Diclofenac has been widely used in clinical practice and is considered to be an effective and well-tolerated medication for managing pain and inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 35333-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,3 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35333-17:
(7*3)+(6*5)+(5*3)+(4*3)+(3*3)+(2*1)+(1*7)=96
96 % 10 = 6
So 35333-17-6 is a valid CAS Registry Number.

35333-17-6Downstream Products

35333-17-6Relevant academic research and scientific papers

Electrooxidative formation of 1,2-diaroylcyclopropanes from 1,3-diaroylpropanes in the presence of KI

Okimoto, Mitsuhiro,Takahashi, Yukio,Kakuchi, Toyoji

, p. 207 - 208 (2007/10/03)

Various 1,2-diaroylcyclopropanes were obtained in good yields by the indirect electrochemical oxidation of 1,3-diaroylpropanes in the presence of catalytic amounts of KI under very mild conditions.

Highly Selective Aldol Reaction of Dibenzoylmethanes with Formaldehyde Catalyzed by Cobalt Schiff Base Complex under Neutral Conditions

Maruyama, Kazushige,Kubo, Katsunobu,Toda, Yukinobu,Kawase, Kazuhiko,Mashino, Takahiro,Nishinaga, Akira

, p. 5609 - 5612 (2007/10/02)

Coordinatively saturated hydroxocobalt(III) Schiff base complexes catalyze highly selective aldol reaction of dibenzoylmethanes with formaldehyde in methanol to give 1,3-dibenzoylpropanes, resulting from retro-Claisen reaction of 1,1,3,3-tetrabenzoylpropanes, which are obtained quantitatively in dichlorometane.Coordinatively saturated cobalt(III) Schiff base complexes ligating a substrate anion as a monodentate ligand is found to be the reactive species.

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