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α-Hydroxy-3-phenoxypropiophenone dimethyl acetal is a complex organic compound with the molecular formula C17H18O4. It is a derivative of propiophenone, featuring a hydroxyl group (-OH) and a phenoxy group (C6H5O-) attached to the molecule. The dimethyl acetal functional group is formed by the reaction of the hydroxyl group with two methanol molecules, resulting in a stable six-membered ring structure. α-hydroxy-3-phenoxypropiophenone dimethyl acetal is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides. Due to its chemical complexity, it is typically synthesized in a controlled laboratory environment and requires careful handling due to its potential reactivity.

85225-11-2

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85225-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85225-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,2 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85225-11:
(7*8)+(6*5)+(5*2)+(4*2)+(3*5)+(2*1)+(1*1)=122
122 % 10 = 2
So 85225-11-2 is a valid CAS Registry Number.

85225-11-2Relevant academic research and scientific papers

An efficient synthesis of fenoprofen, an important antiinflammatory agent

Sonawane, H. R.,Nanjundiah, B. S.,Nazeruddin, G. M.

, p. 705 - 706 (2007/10/02)

A simple and practical synthesis of (+/-)-fenoprofen, a well-known non-steroidal antiinflammatory agent, from the commercially available m-phenoxybenzaldehyde has been described.

Manufacture of alpha-arylalkanoic acids and precursors

-

, (2008/06/13)

α-Arylalkanoic acids or esters, orthoesters or amides thereof are prepared by forming an α-hydroxy ketal or thioketal of an aryl alkyl ketone, activating the α-hydroxy substituent with an esterifying agent to form the corresponding ketal or thioketal ester substrate, wherein the ester group is sufficiently labile to non-catalytically disassociate from the substrate in a protic or dipolar, aprotic solvent, maintaining the ester substrate in contact with the protic or dipolar, aprotic solvent or mixtures thereof for a time sufficient to form the corresponding α-arylakanoic acid or ester, orthoester or amide thereof, and optionally concomitantly or sequentially hydrolyzing any ester, orthoester or amide formed to the corresponding α-arylalkanoic acid.

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