64267-12-5

Usage

Uses

Used in Photopolymer Imaging:
3-Benzoyl-7-methoxycoumarin is used as a photosensitizer in photopolymer imaging due to its ability to absorb light and initiate the polymerization process. This application is particularly useful in the field of 3D printing and microfabrication, where precise control over the polymerization process is required.
Used in Pharmaceutical Industry:
3-Benzoyl-7-methoxycoumarin is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
As a coumarin derivative, 3-Benzoyl-7-methoxycoumarin is used in chemical research to study the properties and reactions of coumarin compounds. This research can lead to the discovery of new compounds with potential applications in various fields.
Used in Analytical Chemistry:
3-Benzoyl-7-methoxycoumarin can be used as a fluorescent marker or probe in analytical chemistry. Its ability to emit light upon exposure to specific wavelengths of light makes it a valuable tool for detecting and analyzing various substances.
Used in Material Science:
The unique properties of 3-Benzoyl-7-methoxycoumarin can also be utilized in the development of new materials with specific characteristics, such as light-sensitive materials or materials with enhanced optical properties.

InChI:InChI=1/C17H12O4/c1-20-13-8-7-12-9-14(17(19)21-15(12)10-13)16(18)11-5-3-2-4-6-11/h2-10H,1H3

Upstream product

• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 614-16-4 Benzoylacetonitrile 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 97139-82-7 o-acetoxypropiophenone 
• 531-59-9 7-methoxycoumarin 
• 100-52-7 benzaldehyde 
• 100-51-6 benzyl alcohol 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 

Downstream Products

• 1194476-82-8 (E)-3-benzoyl-4-(dec-1-enyl)-7-methoxychroman-2-one 
• 1194476-66-8 (3R,4S)-3-benzoyl-4-ethyl-7-methoxychroman-2-one 
• 1428239-00-2 3-benzoyl-4-cyano-7-methoxycoumarin 
• 1428239-01-3 3-benzoyl-4-carboxy-7-methoxycoumarin 

Relevant academic research and scientific papers

Coumarin derivatives act as novel inhibitors of human dipeptidyl peptidase III: Combined in vitro and in silico study

Dipeptidyl peptidase III (DPP III), a zinc-dependent exopeptidase, is a member of the metalloproteinase family M49 with distribution detected in almost all forms of life. Although the physiological role of human DPP III (hDPP III) is not yet fully elucida

Ros inhibitory activity and cytotoxicity evaluation of benzoyl, acetyl, alkyl ester, and sulfonate ester substituted coumarin derivatives

Background: A number of non-steroidal anti-inflammatory drugs (NSAIDs) including aspirin, indomethacin, ibuprofen, flufenamic acid, and phenylbutazone are being clinically used to treat inflammatory disorders. These NSAIDs are associated with serious side

A Regioselective Approach to C3-Aroylcoumarins via Cobalt-Catalyzed C(sp 2)-H Activation Carbonylation of Coumarins

A new cobalt-catalyzed C-H bond activation of coumarins with aryl halides or pseudohalides and carbon monoxide insertion to give various 3-aroylcoumarin derivatives is described. It is the first time that CO as C1 feedstock is used as the coupling partners in cobalt-catalyzed regioselective coumarin C-H functionalization reactions. Upon activation with manganese powder, the Co catalyzes the C-H bond activation carbonylation reactions of aryl iodides, bromides, and even triflates under mild conditions, providing the regioselective aroylated products in moderate to good yields.

Palladium-Catalyzed Carbonylation of Coumarin C(sp 2)-H Bonds: A New Entry to Arylcoumarin Ketones

A facile and efficient palladium-catalyzed carbonylation of coumarins involving two C-C bond formations has been developed. The C-H bond oxidative functionalization proceeds through aroylation with insertion of carbon monoxide to give arylcoumarin ketones

Metal-Free, Regioselective, Dehydrogenative Cross-Coupling between Formamides/Aldehydes and Coumarins by C–H Functionalization

A highly efficient, single-step, metal-free synthetic approach to the synthesis of coumarin-3-carboxamides has been developed. The protocol employs tert-butyl peroxybenzoate as a radical initiator to achieve the regioselective carboxamidation of coumarins at C-3 in good-to-moderate yields. The established reaction protocol offers a wide substrate scope as it allows the use of both formamides as well as aldehydes as coupling partners with excellent regioselectivity. Furthermore, mechanistic investigations illustrate that the reaction proceeds by a free-radical pathway.

Anti-MRSA (Multidrug resistant Staphylococcus aureus) activity of 3-substituted coumarins

Background: Infectious pathogenic bacteria are the key virulence in our daily life. Especially diseases produced by multidrug resistant Staphylococcus aureus (MRSA) still contributing in morbidity and mortality in humans. Discovery of new and safer antibi

A Regioselective Metal-Free Construction of 3-Aroyl Coumarins by Csp2-H Functionalization

A successive metal-free TBHP-mediated regioselective C-H functionalization of coumarins toward expedient synthesis of 3-aroyl coumarins is unveiled. The ongoing method conducted through the reaction of either coumarins or coumarin-3-carboxylic acids with

Iron-catalyzed regioselective direct coupling of aromatic aldehydes with coumarins leading to 3-aroyl coumarins

An efficient protocol for iron-catalyzed cross-coupling of coumarins with aromatic aldehydes has been developed. The various 3-aroyl coumarins were selectively afforded in moderate yields. Some notable features of this protocol are high efficiency, wide f

3-KETOCOUMARINES FOR LED PHOTOCURING

The present invention relates to 3-ketocoumarines which can be used as photoinitiators in LED photocuring and to a process for curing compositions comprising said 3-ketocoumarines.

KETOCOUMARINS AS PHOTOINITIATORS AND PHOTOSENSITIZERS IN INKS

A series of novel ketocoumarin photoinitiators are disclosed for use in radiation curing.