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Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2,5'-Dihydroxy acetophenone is used as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the development of new compounds with therapeutic and pesticidal properties, contributing to the advancement of these industries.
Used in Cosmetic Industry:
2,5'-Dihydroxy acetophenone is used as an active ingredient in cosmetic products for its potential antioxidant and anti-inflammatory properties. It may help protect the skin from oxidative stress and inflammation, promoting healthier and more youthful-looking skin.
Used in Healthcare Industry:
In the healthcare industry, 2,5'-dihydroxy acetophenone is being explored for its potential health benefits. Its antioxidant and anti-inflammatory properties may contribute to the prevention and treatment of various diseases and conditions, such as inflammation-related disorders and oxidative stress-related diseases.
Used in Organic Compound Synthesis:
2,5'-Dihydroxy acetophenone is used as a key intermediate in the synthesis of other organic compounds. Its versatile chemical structure allows for the creation of a wide range of compounds with diverse applications in various fields, including materials science, chemical engineering, and environmental science.
Ongoing Research:
2,5'-Dihydroxy acetophenone is the subject of ongoing research to fully understand its range of properties and potential uses. As new applications and benefits are discovered, its importance in various industries is expected to grow, further expanding its utility and impact on human health and technological advancements.

Upstream product

• 620-17-7 3-ethylphenol 
• 123-31-9 hydroquinone 
• 1205-91-0 benzene-1,4-diyl diacetate 

Downstream Products

• 869478-09-1 8-acetyl-6-(phenylmethoxy)-4H-1,4-benzoxazin-3-one 
• 926319-53-1 8-(bromoacetyl)-6-(phenylmethoxy)-2H-1,4-benzoxazin-3(4H)-one 

Relevant academic research and scientific papers

Selective oxidation of aliphatic C-H bonds in alkylphenols by a chemomimetic biocatalytic system

Selective oxidation of aliphatic C-H bonds in alkylphenols serves significant roles not only in generation of functionalized intermediates that can be used to synthesize diverse downstream chemical products, but also in biological degradation of these environmentally hazardous compounds. Chemo-, regio-, and stereoselectivity; controllability; and environmental impact represent the major challenges for chemical oxidation of alkylphenols. Here, we report the development of a unique chemomimetic biocatalytic system originated from the Gram-positive bacterium Corynebacterium glutamicum. The system consisting of CreHI (for installation of a phosphate directing/ anchoring group), CreJEF/CreG/CreC (for oxidation of alkylphenols), and CreD (for directing/anchoring group offloading) is able to selectively oxidize the aliphatic C-H bonds of p-And m-Alkylated phenols in a controllable manner. Moreover, the crystal structures of the central P450 biocatalyst CreJ in complex with two representative substrates provide significant structural insights into its substrate flexibility and reaction selectivity.

Beta2-receptorexcitant and preparation method and application thereof

The invention relates to a following formula I showed compound in a free form, a salt form or a solvated form and having a beta2-receptor exciting effect. II and III are contained in R1, Ar are following formula groups IV and V, definition of R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R13, R14, R15, R16, m and o is shown in the description. The invention further relates to a preparation method of the compound and application of a compound serving as a drug, in particular to treatment of diseases such as a chronic obstructive pulmonary disease, asthma and heart failure the aspects of a respiratory and cardiovascular system and a cardiovascular system.