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Usage

Uses

Used in Pharmaceutical Industry:
Piceol is used as a therapeutic agent for its potential in treating various diseases, including cancer and cardiovascular disorders, due to its antioxidant and anti-inflammatory properties.
Used in Nutraceutical Industry:
Piceol can be used as a dietary supplement or functional food ingredient, leveraging its health-promoting properties to support overall well-being and disease prevention.
Used in Cosmetic Industry:
Given its antioxidant properties, piceol can be utilized in cosmetic products to protect the skin from oxidative stress and promote a youthful appearance.
Used in Agricultural Industry:
Piceol's natural occurrence and potential anti-inflammatory properties may find applications in agricultural settings, such as in the development of plant protectants or animal health products.
Note: The uses listed are speculative and based on the general properties of piceol mentioned in the provided materials. Actual applications may vary and would require further research, development, and regulatory approval.

Upstream product

• 5298-27-1 (2,4-dihydroxyphenyl)(4-methoxyphenyl)methanone 
• 74-88-4 methyl iodide 
• 108-46-3 recorcinol 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 696-62-8 para-iodoanisole 
• 100-07-2 4-methoxy-benzoyl chloride 
• 151-10-0 1,3-Dimethoxybenzene 
• 100-09-4 4-methoxybenzoic acid 
• 1470-79-7 2,4,4'-trihydroxy-benzophenone 
• 4038-15-7 2,4,4'-trimethoxybenzophenone 
• 74-83-9 methyl bromide 
• 2237-36-7 4-methoxysalicylic acid 
• 100-66-3 methoxybenzene 

Downstream Products

• 52871-37-1 6-methoxy-3-(4-methoxy-phenyl)-benzofuran-2-carboxylic acid ethyl ester 
• 35983-60-9 6-methoxy-3-(4-methoxy-phenyl)-benzofuran-2-carboxylic acid 
• 60312-34-7 6-methoxy-3-(4-methoxy-phenyl)-benzofuran-2-carbaldehyde 
• 75226-99-2 [5-methoxy-2-(4-methoxy-benzoyl)-phenoxy]-acetic acid 
• 52814-52-5 3-(4-methoxyphenyl)-6-methoxy-1-benzofuran 
• 679410-96-9 4-[5-methoxy-2-(4-methoxybenzyl)phenoxy]phenol 
• 143286-73-1 (2-Hydroxy-4-methoxy-phenyl)-(4-methoxy-phenyl)-methanone oxime 

Relevant academic research and scientific papers

Directed Hydroxylation of sp2 and sp3 C-H Bonds Using Stoichiometric Amounts of Cu and H2O2

The use of copper for C-H bond functionalization, compared to other metals, is relatively unexplored. Herein, we report a synthetic protocol for the regioselective hydroxylation of sp2 and sp3 C-H bonds using a directing group, stoichiometric amounts of Cu and H2O2. A wide array of aromatic ketones and aldehydes are oxidized in the carbonyl γ-position with remarkable yields. We also expanded this methodology to hydroxylate the β-position of alkylic ketones. Spectroscopic characterization, kinetics, and density functional theory calculations point toward the involvement of a mononuclear LCuII(OOH) species, which oxidizes the aromatic sp2 C-H bonds via a concerted heterolytic O-O bond cleavage with concomitant electrophilic attack on the arene system.

Rhodium-Catalyzed Directing-Group-Assisted Aldehydic C–H Arylations with Aryl Halides

A rhodium-catalyzed general protocol for the directing-group-assisted arylation of aromatic aldehydic C–H bonds was developed. This method involves either hydroxy- or amino-group-directed aldehyde C–H arylation with various aryl halides. A broad synthetic scope for the preparation of 2-hydroxybenzophenones was established with electronically variant salicylaldehydes and aryl halides with chemo- and regioselective possibilities. The developed protocol was also applied in the synthesis of medicinally important 3-salicyloylpyridines in high yields.

Palladium-catalyzed ortho-CH-bond oxygenation of aromatic ketones

A palladium-catalyzed C(sp2)-H bond oxygenation reaction is described. This protocol represents the first example of a C-H bond cleavage/C-O bond formation sequence, by employing a ketone moiety as the directing group. With this new catalytic method, a variety of ortho-acylphenols can be easily accessed from arylketones.

A new series of estrogen receptor modulators: Effect of alkyl substituents on receptor-binding affinity

New types of selective estrogen receptor modulators (SERMs) were synthesized and evaluated for their binding affinity and biological effect on reproductive cells. A proposed lead structure (B) was derivatized to provide compounds 30 and 44, which showed g

SUNSCREEN COMPOSITIONS

The present invention relates to improved sunscreen compositions, more preferably to improved sunscreen compositions containing at least one sunscreening agent (sunscreen) and a silicone-polyamide copolymer.

BeCl2 as a new highly selective reagent for dealkylation of aryl-methyl ethers

An efficient and simple method is introduced for the selective removal of methyl group from poly aryl-methyl ethers, in some important derivatives of benzophenones, xanthones, anthraquinones, aryl esters, benzamides and nitroanisoles with BeCl2.

Synthese von 4-Alkoxy-2-hydroxyphenylketoximen als Metallextraktions-Reagenzien

The C-Acylation (Friedel-Crafts reaction) of resorcinol with aluminium chloride, the monoetherification in 4-position of the resulting 2,4-dihydroxyphenylketones, and the preparation of oximes (8, 9, 10, 11) from this ketones were investigated.The compounds obtained are characterized by elemental analysis, and the i.r., u.v. and 1H-n.m.r. spectra are discussed.Solubility data of some oximes are determined in water, octane and toluene.The extraction properties for copper-(II)-and iron-(III)-ions are measured by isotope methods in relation to the extragent structure, the extraction time and the pH-range.