74815-88-6

Usage

Molecular weight

368.38 g/mol

Appearance

Yellow crystalline powder

Solubility

Insoluble in water, soluble in organic solvents (e.g., ethanol, dichloromethane)

Functional groups

Ketone, phenol, and alkene groups are present in the molecule.
Curcumin is the active component of turmeric, which is a spice derived from the rhizomes of the plant Curcuma longa.
Known for its anti-inflammatory, antioxidant, and potential anti-cancer properties.
Being investigated for its potential use in the treatment of various diseases and conditions, such as Alzheimer's disease, arthritis, and cancer.
Curcumin is an important compound in the field of medicinal chemistry due to its wide range of potential health benefits.

Upstream product

• 106627-40-1 4-(allyloxy)-2-hydroxypropiophenone 
• 5792-36-9 2',4'-dihydroxypropiophenone 

Downstream Products

• 79558-49-9 2,4-dihydroxy-3-propylphenyl ethyl ketone 
• 18651-21-3 8-allyl-7-hydroxy-3-methyl-2-phenyl-chromen-4-one 
• 124210-95-3 3-Methyl-2-phenyl-4H-furo<2,3-h><1>benzopyran-4-one 
• 106627-30-9 diphenylmethyl 6-(4'-propanoyl-3'-hydroxy-2'-propylphenoxy)hexanoate 
• 92518-45-1 6-(4-Propionyl-3-hydroxy-2-propylphenoxy)hexanoic acid 
• 194608-85-0 {3-Chloro-4-[3-(3-hydroxy-4-{1-[(E)-hydroxyimino]-propyl}-2-propyl-phenoxy)-propylsulfanyl]-phenyl}-acetic acid methyl ester 
• 194608-84-9 methyl 3-chloro-4-(3-(2-propyl-3-hydroxy-4-propionylphenoxy)propylthio)phenylacetate 
• 194608-87-2 {3-chloro-4-[3-(3-ethyl-7-propyl-benzo[d]isoxazol-6-yloxy)-propylsulfanyl]-phenyl}-acetic acid methyl ester 

Relevant academic research and scientific papers

Phenylacetic acid derivatives as hPPAR agonists

Beginning with the weakly active lead structure 1, a new series of hPPAR agonists was developed. In vivo glucose and triglyceride lowering activity was obtained by homologation and oxamination to 3, then conversion to substituted benzisoxazoles 4 and 5. F

Leukotriene receptor antagonists. 1. Synthesis and structure-activity relationships of alkoxyacetophenone derivatives

A series of derivatives of 2,4-dihydroxy-3-propylacetophenone were prepared and examined for their ability to block leukotriene D4 (LTD4) induced contraction of guinea pig ileum. Straight-chain carboxylic acids where the carboxyl gro