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2-(4-butoxy)phenylpropionic acid is an organic compound with the chemical formula C13H18O4. It is a derivative of phenylpropionic acid, featuring a butoxy group (C4H9O) attached to the para position of the phenyl ring. 2-(4-butoxy)phenylpropionic acid is characterized by its molecular weight of 242.28 g/mol and a melting point of approximately 70-72°C. It is a white crystalline solid and is soluble in organic solvents such as ethanol and acetone. 2-(4-butoxy)phenylpropionic acid is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its properties, such as its ability to form salts and esters, make it a versatile building block in the chemical industry.

3585-71-5

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3585-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3585-71-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3585-71:
(6*3)+(5*5)+(4*8)+(3*5)+(2*7)+(1*1)=105
105 % 10 = 5
So 3585-71-5 is a valid CAS Registry Number.

3585-71-5Relevant academic research and scientific papers

In Vivo Characterization of Hydroxamic Acid Inhibitors of 5-Lipoxygenase

Summers, James B.,Gunn, Bruce P.,Mazdiyasni, Hormoz,Goetze, Andrew M.,Young, Patrick R.,et al.

, p. 2121 - 2126 (2007/10/02)

The hydroxamic acid functionality can be incorporated into simple molecules to produce potent inhibitors of 5-lipoxygenase.The ability of many of these hydroxamates to inhibit leukotriene synthesis in vivo has been measured directly with a rat peritoneal anaphylaxis model.Despite their potent enzyme inhibitory activity in vitro, many orally dosed hydroxamic acids only weakly inhibited leukotriene synthesis in vivo.This discrepancy is attributable at least in part to the rapid metabolism of hydroxamates to the corresponding carboxylic acids, which are inactive against the enzyme.A study of the structural features that affect this metabolism revealed that 2-arylpropionohydroxamic acids are relatively resistant to metabolic hydrolysis.Several members of this class of hydroxamates are described that are orally active inhibitors of leukotriene synthesis.

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