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2,4-dichloro-3,5-diethoxyphenol is a chemical compound characterized by the molecular formula C10H12Cl2O3. It is an organic compound that manifests as a white crystalline solid, exhibiting solubility in organic solvents while remaining insoluble in water. 2,4-dichloro-3,5-diethoxyphenol is recognized for its selective action against a variety of weeds, making it a valuable asset in the agricultural and horticultural sectors.

38730-43-7

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38730-43-7 Usage

Uses

Used in Agricultural Applications:
2,4-dichloro-3,5-diethoxyphenol is utilized as a herbicide for its ability to selectively target and control a broad spectrum of weeds. It operates by disrupting the hormonal balance of unwanted plants, thereby inhibiting their growth and allowing for more manageable and productive agricultural landscapes.
Used in Horticultural Applications:
In horticulture, 2,4-dichloro-3,5-diethoxyphenol serves as a pesticide, helping to maintain the aesthetic and health of gardens and landscapes by preventing the overgrowth of weeds that can compete with desired plant species for nutrients and space.
It is crucial to handle 2,4-dichloro-3,5-diethoxyphenol with caution due to its potential harmful effects if ingested, inhaled, or if it comes into contact with the skin or eyes, underscoring the need for proper safety measures during its application.

Check Digit Verification of cas no

The CAS Registry Mumber 38730-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,3 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38730-43:
(7*3)+(6*8)+(5*7)+(4*3)+(3*0)+(2*4)+(1*3)=127
127 % 10 = 7
So 38730-43-7 is a valid CAS Registry Number.

38730-43-7Relevant academic research and scientific papers

2-(Aminomethyl)phenols, a new class of saluretic agents. I. Effect of nuclear substitution

Stokker,Deana,deSolms,Schultz,Smith,Cragoe Jr.,Baer,Ludden,Russo,Scriabine,Sweet,Watson

, p. 1414 - 1427 (2007/10/02)

A series of 2-(aminomethyl)phenols was synthesized and tested in rats and dogs for saluretic and diuretic activity. A number of these compounds exhibit a high order of activity on iv or po administration. The most active compounds belong to a subseries of 4-alkyl-6-halo derivatives of which 2,2(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenyl, is the most active. Compound 2 also possesses significant antihypertensive activity, an adjunctive pharmacological parameter which distinguishes 2 from the other compounds prepared in this series. In addition, 2 displays both topical saluretic and antiinflammatory activities.

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