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(4-ISOPROPOXY-BENZOYLAMINO)-ACETIC ACID, also known as ibufenac, is a non-steroidal anti-inflammatory drug (NSAID) characterized by its anti-inflammatory and analgesic properties. It is effective in managing mild to moderate pain and inflammation, making it a valuable compound for various medical applications.

51220-54-3

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51220-54-3 Usage

Uses

Used in Pharmaceutical Industry:
(4-ISOPROPOXY-BENZOYLAMINO)-ACETIC ACID is used as an anti-inflammatory and analgesic agent for the relief of mild to moderate pain and inflammation associated with conditions such as arthritis, menstrual cramps, and musculoskeletal injuries. It achieves this by inhibiting the production of prostaglandins, which are chemical messengers that contribute to pain and inflammation in the body.
However, it is important to note that, like other NSAIDs, (4-ISOPROPOXY-BENZOYLAMINO)-ACETIC ACID can pose certain risks and side effects, such as gastrointestinal irritation and an increased risk of cardiovascular events, especially with long-term use and high doses. Therefore, it is crucial to use this chemical under the guidance of a healthcare professional and to adhere to the recommended dosage and duration of treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 51220-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,2 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51220-54:
(7*5)+(6*1)+(5*2)+(4*2)+(3*0)+(2*5)+(1*4)=73
73 % 10 = 3
So 51220-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO4/c1-8(2)17-10-5-3-9(4-6-10)12(16)13-7-11(14)15/h3-6,8H,7H2,1-2H3,(H,13,16)(H,14,15)

51220-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-propan-2-yloxybenzoyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names 4-hydroxybenzoyl-glycine isopropyl ether

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:51220-54-3 SDS

51220-54-3Downstream Products

51220-54-3Relevant academic research and scientific papers

Polymer-Supported Mitsunobu Ether Formation and its Use in Combinatorial Chemistry

Krchnak, Viktor,Flegelova, Zuzka,Weichsel, Aleksandra S.,Lebl, Michal

, p. 6193 - 6196 (2007/10/02)

Aromatic hydroxy acids have been attached to a polymeric solid support and the phenolic hydroxy groups have been reacted with a variety of primary and secondary alcohols under the conditions of the Mitsunobu reaction (triphenylphosphine and diethyl azodicarboxylate) in tetrahydrofuran.In most cases the reaction provided a nearly quantitative yield of alkyl aryl ethers, as determined after cleaving theproduct from the resin.To demonstrate that the polymer-supported Mitsunobu reaction is useful for combinatorial library synthesis, we synthesized a number of model compounds and a simple three randomization step library composed of 4,200 different compounds.

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