Welcome to LookChem.com Sign In|Join Free
  • or
5-(4-(Acetylamino)phenyl)-1H-imidazole-2-acetic acid ethyl ester, also known as ethyl 5-(4-acetamidophenyl)-1H-imidazole-2-acetate, is a synthetic organic compound with the molecular formula C14H16N2O3. It is a derivative of imidazole and is characterized by its strong antiproliferative and anti-inflammatory properties. 5-(4-(Acetylamino)phenyl)-1H-imidazole-2-acetic acid ethyl ester is commonly used in pharmaceutical research and has been studied for its potential applications in treating various medical conditions, including cancer and inflammatory diseases. The ethyl ester form of the compound enhances its solubility and bioavailability, making it a promising candidate for further drug development.

908007-24-9

Post Buying Request

908007-24-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

908007-24-9 Usage

Uses

Used in Pharmaceutical Research:
5-(4-(Acetylamino)phenyl)-1H-imidazole-2-acetic acid ethyl ester is used as a research compound for its potential applications in the treatment of various medical conditions. Its strong antiproliferative and anti-inflammatory properties make it a promising candidate for drug development.
Used in Cancer Treatment:
In the field of oncology, 5-(4-(Acetylamino)phenyl)-1H-imidazole-2-acetic acid ethyl ester is used as a potential therapeutic agent for the treatment of various types of cancer. Its antiproliferative properties can help inhibit the growth and progression of cancer cells.
Used in Inflammatory Disease Treatment:
5-(4-(Acetylamino)phenyl)-1H-imidazole-2-acetic acid ethyl ester is also used in the treatment of inflammatory diseases due to its potent anti-inflammatory properties. It can help alleviate inflammation and reduce the severity of symptoms associated with these conditions.
Used in Drug Development:
As a synthetic derivative of imidazole, 5-(4-(Acetylamino)phenyl)-1H-imidazole-2-acetic acid ethyl ester is used in the development of new pharmaceutical agents. Its improved solubility and bioavailability compared to other forms of the compound make it a valuable asset in the creation of more effective and targeted treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 908007-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,0,0 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 908007-24:
(8*9)+(7*0)+(6*8)+(5*0)+(4*0)+(3*7)+(2*2)+(1*4)=149
149 % 10 = 9
So 908007-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H17N3O3/c1-3-21-15(20)8-14-16-9-13(18-14)11-4-6-12(7-5-11)17-10(2)19/h4-7,9H,3,8H2,1-2H3,(H,16,18)(H,17,19)

908007-24-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[5-(4-acetamidophenyl)-1H-imidazol-2-yl]acetate

1.2 Other means of identification

Product number -
Other names 5-[4-(Acetylamino)phenyl]-1H-imidazole-2-acetic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:908007-24-9 SDS

908007-24-9Downstream Products

908007-24-9Relevant academic research and scientific papers

Efficient synthesis of 2-imidazol-2-ylacetates

Ha, Jae Du,Lee, Su Jung,Nam, So Yeun,Kang, Seung Kyu,Cho, Seung Yoon,Ahn, Jin Hee,Choi, Joong-Kwon

, p. 6201 - 6204 (2007/10/03)

A simple method of synthesizing various 2-imidazol-2-ylacetates is described. Condensation of α-aminoketals with imidates, followed by cyclization in refluxing 4 M-HCl/Dioxane, yielded 2-imidazol-2-ylacetates under one-pot and mild reaction conditions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 908007-24-9