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2-(3-BENZYLOXYPHENYL)PROPIONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56911-49-0

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56911-49-0 Usage

Medicinal use

Relieves pain, reduces inflammation, and lowers fever

Drug class

Nonsteroidal anti-inflammatory drugs (NSAIDs)

Mechanism of action

Inhibits the production of certain chemicals in the body that cause pain and inflammation

Commonly prescribed for

Arthritis, menstrual cramps, and muscle aches

Available forms

Tablets, capsules, and liquid suspension

Safety and effectiveness

Generally considered safe and effective when used as directed

Side effects

May cause stomach upset, dizziness, and increased risk of heart attack or stroke at high doses or prolonged use

Importance of professional guidance

Use under the guidance of a healthcare professional to minimize potential risks and maximize its benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 56911-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56911-49:
(7*5)+(6*6)+(5*9)+(4*1)+(3*1)+(2*4)+(1*9)=140
140 % 10 = 0
So 56911-49-0 is a valid CAS Registry Number.

56911-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-phenylmethoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2-(2,4-DIBROMOPHENYL)-1,2-DIHYDRO-5-PHENYL-3H-1,2,4-TRIAZOL-3-ONE

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:56911-49-0 SDS

56911-49-0Downstream Products

56911-49-0Relevant academic research and scientific papers

Iron-catalyzed, highly regioselective synthesis of α-aryl carboxylic acids from styrene derivatives and CO2

Greenhalgh, Mark D.,Thomas, Stephen P.

, p. 11900 - 11903 (2012/09/07)

The iron-catalyzed hydrocarboxylation of aryl alkenes has been developed using a highly active bench-stable iron(II) precatalyst to give α-aryl carboxylic acids in excellent yields and with near-perfect regioselectivity. Using just 1 mol % FeCl2, bis(imino)pyridine 6 (1 mol %), CO 2 (atmospheric pressure), and a hydride source (EtMgBr, 1.2 equiv), a range of sterically and electronically differentiated aryl alkenes were transformed to the corresponding α-aryl carboxylic acids (up to 96% isolated yield). The catalyst was found to be equally active with a loading of 0.1 mol %. Preliminary mechanistic investigations show that an iron-catalyzed hydrometalation is followed by transmetalation and reaction with the electrophile (CO2).

M-phenoxyphenyl propionic acid derivatives and preparation thereof

-

, (2008/06/13)

New meta-phenoxyphenyl propionic acid derivatives and pharmacologically acceptable salts thereof having excellent anti-inflammatory and analgesic activities with low toxicity are provided. The new compounds are adapted for therapeutical treatment of various inflammatory diseases by oral administration without injurious by-effects; successive administrations for an elongated period are not accompanied with an appreciable gastric irritability and the like.

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