23107-96-2

Basic information

• Product Name: 2-Benzoylbenzeneacetic acid
• Synonyms: (2-Benzoylphenyl)acetic acid;2-Benzoylbenzeneacetic acid;2-Benzoylphenylacetic acid;2-BPAA;RU-5045
• CAS NO: 23107-96-2
• Molecular Formula: C₁₅H₁₂O₃
• Molecular Weight: 240.27
• Mol File: 23107-96-2.mol
• Article Data: 12

Chemical Properties

• Melting Point: 139 °C
• Boiling Point: 342.97°C (rough estimate)
• Flash Point: 245.7°C
• Appearance: /
• Density: 1.1783 (rough estimate)
• Vapor Pressure: 3.11E-09mmHg at 25°C
• Refractive Index: 1.5570 (estimate)
• PKA: 4.13±0.10(Predicted)
• CAS DataBase Reference: 2-Benzoylbenzeneacetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Benzoylbenzeneacetic acid(23107-96-2)
• EPA Substance Registry System: 2-Benzoylbenzeneacetic acid(23107-96-2)

Safety Data

• Hazardous Substances Data: 23107-96-2(Hazardous Substances Data)

Usage

Safety Profile

Poison by intraperitoneal route.Moderately toxic by ingestion. When heated todecomposition it emits acrid smoke and irritating fumes.

InChI:InChI=1/C15H12O3/c16-14(17)10-12-8-4-5-9-13(12)15(18)11-6-2-1-3-7-11/h1-9H,10H2,(H,16,17)

Upstream product

• 1961-97-3 3-phenyl-1H-indene 
• 64655-21-6 α-hydroxydecyl hydroperoxide 
• 87943-83-7 1-Phenyl-9,10,11-trioxa-tricyclo[6.2.1.0^2,7]undeca-2,4,6-triene 
• 67-64-1 acetone 
• 108-86-1 bromobenzene 
• 27419-23-4 methyl 2-(2-benzoylphenyl) acetate 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 19164-61-5 7-phenylbicyclo<4.2.0>octa-1,3,5-trien-7-ol 
• 124-38-9 carbon dioxide 
• 131-58-8 2-Methylbenzophenone 
• 83-33-0 inden-1-one 
• 36374-47-7 1-hydroxy 1-phenyl indane 
• 703-59-3 homophthalic anhydride 
• 71-43-2 benzene 

Downstream Products

• 154502-70-2 ethyl 2-(2-benzoylphenyl)acetate 
• 35011-63-3 1-phenyl-3,5-dihydro-benzo[d][1,2]diazepin-4-one 
• 95965-83-6 1-phenyl-4-(N'-phenylpiperazino)-3-isochroman 
• 95965-63-2 methyl-3-phenyl-1,3-dihydroisobenzofuran-1-carboxylate 
• 42710-67-8 4-dimethylamino-1-phenylisochroman 
• 95965-67-6 4-dimethylamino-1-phenyl-3-isochromanone 
• 95965-65-4 1-carbamoyl-3-phenyl-1,3-dihydroisobenzofuran 
• 95965-75-6 1-phenyl-4-(N'-phenylpiperazino)-3-isochromanone 
• 95965-73-4 1-phenyl-4-(N'-methylpiperazino)-3-isochromanone 
• 95965-81-4 1-phenyl-4-(N'-methylpiperazino)-3-isochroman 
• 95965-55-2 3-Phenyl-1,3-dihydro-isobenzofuran-1-carbonyl chloride 
• 31578-27-5 4-bromo-1-phenyl-3-isochromanone 
• 34958-31-1 1-dimethylcarbamoyl-3-phenyl-1,3-dihydroisobenzofuran 
• 755691-12-4 1-(N,N-dimethylaminomethyl)-3-phenyl-1,3-dihydroisobenzofuran 

Relevant articles and documents

A microfluidic photoreactor enables 2-methylbenzophenone light-driven reactions with superior performance

Light-driven reactions of 2-methylbenzophenones (2-MBPs) occur with improved yields (up to >98%) and reaction rates (up to 0.240 mmol h-1) by using a tailored microfluidic photoreactor (MFP). For the first time, coumarins were converted into 4-

Combined Photoredox/Enzymatic C?H Benzylic Hydroxylations

Chemical transformations that install heteroatoms into C?H bonds are of significant interest because they streamline the construction of value-added small molecules. Direct C?H oxyfunctionalization, or the one step conversion of a C?H bond to a C?O bond, could be a highly enabling transformation due to the prevalence of the resulting enantioenriched alcohols in pharmaceuticals and natural products,. Here we report a single-flask photoredox/enzymatic process for direct C?H hydroxylation that proceeds with broad reactivity, chemoselectivity and enantioselectivity. This unified strategy advances general photoredox and enzymatic catalysis synergy and enables chemoenzymatic processes for powerful and selective oxidative transformations.

GASTRIN AND CHOLECYSTOKININ RECEPTOR LIGANDS

This invention relates to a compound of formula (I) wherein the variables are as defined in the specification. The compound is useful for the treatment of gastrin related disorders.