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(R)-N-(1-(4-hydroxymethylphenyl)ethyl)acetamide is a chemical compound with the molecular formula C11H15NO2. It is an amide derivative that features a chiral center, making it a valuable component in medicinal chemistry research. (R)-N-(1-(4-hydroxymethylphenyl)ethyl)acetamide is widely utilized as a building block for the synthesis of pharmaceuticals due to its unique structure and properties. Additionally, it has demonstrated pharmacological activity, particularly in the realms of analgesia and anti-inflammatory effects, positioning it as a potential candidate for drug development and further exploration in medicinal chemistry and pharmacology.

223514-69-0

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223514-69-0 Usage

Uses

Used in Pharmaceutical Industry:
(R)-N-(1-(4-hydroxymethylphenyl)ethyl)acetamide is used as a building block for the synthesis of pharmaceuticals because of its unique structure and properties. Its chiral center allows for the creation of various enantiomers, which can have different biological activities and therapeutic effects.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-N-(1-(4-hydroxymethylphenyl)ethyl)acetamide is used as a key component in the development of new drugs. Its amide structure and chiral center provide a foundation for designing and synthesizing novel compounds with potential therapeutic applications.
Used in Pain Management:
(R)-N-(1-(4-hydroxymethylphenyl)ethyl)acetamide is used as an analgesic agent, helping to alleviate pain by interacting with the body's pain receptors and pathways. Its effectiveness in pain management makes it a promising candidate for the development of new pain relief medications.
Used in Anti-Inflammatory Applications:
(R)-N-(1-(4-hydroxymethylphenyl)ethyl)acetamide is also used for its anti-inflammatory properties, which can help reduce inflammation and associated discomfort in various conditions. Its potential use in anti-inflammatory drugs highlights the versatility of (R)-N-(1-(4-hydroxymethylphenyl)ethyl)acetamide in the realm of medicinal chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 223514-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,5,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 223514-69:
(8*2)+(7*2)+(6*3)+(5*5)+(4*1)+(3*4)+(2*6)+(1*9)=110
110 % 10 = 0
So 223514-69-0 is a valid CAS Registry Number.

223514-69-0Relevant academic research and scientific papers

Piperazine compounds and medicinal use thereof

-

, (2008/06/13)

The present invention relates to a piperazine compound of the formula wherein R1and R2are each hydrogen, halogen, lower alkyl, lower alkoxy, amino, substituted amino, nitro, hydroxy or cyano, R3, R4and R5are each hydrogen, halogen, lower alkyl, lower alkoxy, nitro, amino, substituted amino or hydroxy, R6and R7are each hydrogen, lower alkyl, lower alkyl substituted by halogen, aralkyl, acyl or lower acyl substituted by halogen, R8and R9are each hydrogen or lower alkyl, Y is lower alkylene and the like, and ring A is phenyl, pyrimidyl, thiazolyl, pyridyl, pyrazyl or imidazolyl, a pharmaceutically acceptable salt thereof and pharmaceutical agents containing these compounds. The compound of the present invention has superior TNF-α production inhibitory effect and/or IL-10 production promoting effect, and, since it is free of or shows only strikingly reduced expression of an effect on the central nervous system, the compound is useful as a highly safe and superior TNF-α production inhibitor an/or IL-10 production promoter and is useful as an agent for the prophylaxis or treatment of various diseases caused by abnormal TNF-α production, diseases curable with IL-10, such as chronic inflammatory diseases, acute inflammatory diseases, inflammatory diseases due to infection, autoimmune diseases, allergic diseases, and TNF-α mediated diseases.

Novel DMARDs on the basis of a new concept of dual cytokine regulation, TNF-α suppression and IL-10 augmentation

Hanano, Tokushi,Adachi, Kunitomo,Aoki, Yoshiyuki,Morimoto, Hiroshi,Naka, Yoichi,Hisadome, Masao,Fukuda, Tetsuko,Sumichika, Hiroshi

, p. 881 - 884 (2007/10/03)

A series of arylpiperazine derivatives was synthesized to obtain agents showing apparent therapeutic effects in a chronic inflammatory animal model, starting from a lead possessing potent dual cytokine regulatory activity in vivo. We found a pyrimidylpipe

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