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64740-36-9

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64740-36-9 Usage

General Description

3-(4-Ethylphenyl)propionic acid, also known as ibuprofen, is a nonsteroidal anti-inflammatory drug (NSAID) commonly used to relieve pain, reduce fever, and decrease inflammation. It works by inhibiting the production of prostaglandins, which are responsible for causing pain and inflammation in the body. Ibuprofen is widely used to treat conditions such as headaches, muscle pain, menstrual cramps, and arthritis. It is available over-the-counter in various forms such as tablets, capsules, and liquid suspensions, and is considered to be an effective and relatively safe medication when used as directed. However, like all medications, ibuprofen can have potential side effects and interactions with other drugs, so it is important to use it under the guidance of a healthcare professional.

Check Digit Verification of cas no

The CAS Registry Mumber 64740-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64740-36:
(7*6)+(6*4)+(5*7)+(4*4)+(3*0)+(2*3)+(1*6)=129
129 % 10 = 9
So 64740-36-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-2-9-3-5-10(6-4-9)7-8-11(12)13/h3-6H,2,7-8H2,1H3,(H,12,13)

64740-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-Ethylphenyl)propionic acid

1.2 Other means of identification

Product number -
Other names 3-(4-ethylphenyl)propanoic acid

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:64740-36-9 SDS

64740-36-9Relevant articles and documents

Improved synthesis of natural ester sintenin and its analogues via Wittig reaction

Sharma, Mukul,Rajesh, U. Chinna,Rawat, Diwan S.

, p. 1853 - 1860 (2014/01/17)

The synthesis of a cytotoxic natural ester sintenin (7a) and twenty eight of its analogues including nitrogen-containing heterocyclic indole moiety (7b-7t), saturated (10a-10d) and unsaturated (10e-10h) amides were carried out by convenient route via one-pot Wittig reaction in aqueous medium with improved yield. A systematic structure activity relationship of sintenin ester was designed by chemically modified derivatives in order to get better cytotoxicity.

MELATONERGIC INDANYL PIPERAZINES

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, (2008/06/13)

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