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Acetamide, N-[4-ethoxy-3,5-bis(1-methylethyl)phenyl]-, also known as N-(4-ethoxy-3,5-diisopropyphenyl)acetamide, is an organic compound with the chemical formula C16H23NO2. It is a derivative of acetamide, featuring a phenyl ring with two isopropyl groups at the 3 and 5 positions, and an ethoxy group at the 4 position. Acetamide, N-[4-ethoxy-3,5-bis(1-methylethyl)phenyl]- is characterized by its molecular weight of 259.36 g/mol and a melting point of 68-70°C. It is a white crystalline solid and is soluble in organic solvents. The compound has potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and properties.

1887-86-1

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1887-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1887-86-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1887-86:
(6*1)+(5*8)+(4*8)+(3*7)+(2*8)+(1*6)=121
121 % 10 = 1
So 1887-86-1 is a valid CAS Registry Number.

1887-86-1Downstream Products

1887-86-1Relevant academic research and scientific papers

Design, synthesis and biological testing of a novel series of anti-inflammatory drugs

Duffy,Dearden,Rostron

, p. 1505 - 1514 (2001)

Many of the non-steroidal anti-inflammatory drugs (NSAIDs) currently marketed produce severe gastro-toxic side effects. The benefits of producing NSAIDs without these side effects are obvious, particularly for patients requiring long-term therapy. The aim of this investigation was to produce novel NSAIDs, based on paracetamol, that exhibit little or no gastro-toxicity. The work covers design, synthesis and testing of 13 drug candidates. The analgesic and anti-inflammatory potencies of the drug candidates were measured using the mouse abdominal constriction assay and the carrageenan-induced rat paw oedema assay, respectively. The stomachs of the rats were examined post-mortem, to assess the gastro-toxicity of the drugs. Of the 13 compounds described herein, 11 were shown to possess analgesic activity at 2-10 times the potency of aspirin, while 8 demonstrated anti-inflammatory activity at 3-10 times the potency of aspirin. Significantly, all of the compounds showed very low gastro-toxicity when compared with aspirin. The results of this study indicate that it is possible to develop novel, potent NSAIDs based on the structure of paracetamol. These compounds have the advantage of demonstrating much lower gastro-toxicity than NSAIDs currently available. Drugs of this type may, in future, provide effective treatments for inflammatory disorders.

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