64798-35-2

Usage

Uses

Used in Pain Relief Applications:
Ibuprofen is used as a pain reliever for a variety of conditions, including headaches, muscle aches, back pain, and dental pain. It helps to alleviate discomfort by reducing inflammation and pain signals in the body.
Used in Anti-Inflammatory Applications:
As an anti-inflammatory agent, ibuprofen is effective in reducing inflammation associated with conditions such as arthritis, tendonitis, and bursitis. It works by inhibiting the enzymes responsible for prostaglandin synthesis, thereby decreasing inflammation and associated pain.
Used in Fever Reduction Applications:
Ibuprofen is used to lower fevers by reducing the body's production of prostaglandins, which are involved in the regulation of body temperature. This helps to bring down elevated temperatures and provide relief from fever symptoms.
Used in Menstrual Cramps Relief Applications:
Ibuprofen is used to alleviate menstrual cramps by reducing the prostaglandins that cause uterine contractions and pain during menstruation. It provides relief from the discomfort and pain associated with menstrual periods.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ibuprofen is used as an active ingredient in various formulations, such as tablets, capsules, and suspensions, to treat a range of conditions that involve pain, inflammation, and fever.

Upstream product

• 64798-33-0 2-(3-chloro-phenyl)-2-methyl-propionitrile 
• 14161-84-3 2-(3-chlorophenyl) propanoic acid 
• 74-88-4 methyl iodide 

Downstream Products

• 64798-36-3 2-(3-chloro-phenyl)-2-methyl-propionyl chloride 
• 1035261-92-7 diethyl 2-(2-(3-chlorophenyl)-2-methylpropanoyl)malonate 
• 1225521-01-6 2-(3-chlorophenyl)-2-methylpropanal 

Relevant academic research and scientific papers

BENZAMIDE COMPOUNDS AS ROR GAMMA MODULATORS

The present disclosure is directed to compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein ring A, R1, R2, R3, R4, R5, n and p are as defined herein, which are active as modulators of retinoid-related orphan receptor gamma t (RORγt). These compounds prevent, inhibit, or suppress the action of RORγt and are therefore useful in the treatment of RORγt mediated diseases, disorders, syndromes or conditions such as, e.g., pain, inflammation, COPD, asthma, rheumatoid arthritis, colitis, multiple sclerosis, psoriasis, neurodegenerative diseases and cancer.

Pd(II)-catalyzed enantioselective C-H activation/C-O bond formation: Synthesis of chiral benzofuranones

Pd(II)-catalyzed enantioselective C-H activation of phenylacetic acids followed by an intramolecular C-O bond formation afforded chiral benzofuranones. This reaction provides the first example of enantioselecctive C-H functionalizations through Pd(II)/Pd(IV) redox catalysis.

NAPHTHALENONE COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF

Compounds of Formula (I) and Formula (II) are useful as inhibitors of HIF prolyl hydroxylases. Compounds of Formula(I) and Formula (II) have the following structures, where the definitions of the variables are provided herein.

Process for producing an α-aromatic group substituted alkanoic acid derivative

Compounds having anti-inflammatory and analgesic activity of the formula STR1 are produced from compounds having the formula STR2 by rearrangement in the presence of a base or an amide and (1) X S O X 1 or X S O 2 X 1 where X and X 1 are halogen or trifluoromethyl or (2) sulfur dioxide and halogen.

3-(α,α-Dimethylbenzyl)urea compounds, compositions, and their use as herbicides

A compound of the general formula (I): STR1 wherein X is halogen or trifluoromethyl, n and m are 0 or 1, R1 is lower C1 - C2 alkyl or C1 - C2 alkoxy and R2 is C4 - C5