2346-67-0

Usage

Chemical Family

2-(2,4,6-Trimethylbenzoyl)benzoic acid belongs to the family of benzoic acids.

Derivative

It is a derivative of benzoic acid with a benzoyl group attached to a benzene ring.

Common Use

It is commonly used as a photoinitiator in the manufacturing of various polymers and coatings.

Light Absorption

It is designed to absorb light in the UV range and initiate the polymerization process.

Applications

It is useful in the production of adhesives, inks, and surface coatings.

Thermal Stability

2-(2,4,6-Trimethylbenzoyl)benzoic acid is known for its high thermal stability.

Efficiency

It is a highly efficient photoinitiator, making it a valuable component in various industrial applications.

InChI:InChI=1/C17H16O3/c1-10-8-11(2)15(12(3)9-10)16(18)13-6-4-5-7-14(13)17(19)20/h4-9H,1-3H3,(H,19,20)

Upstream product

• 88-95-9 Phthaloyl dichloride 
• 108-67-8 1,3,5-trimethyl-benzene 
• 3112-46-7 mesitylglyoxylic acid 
• 65-85-0 benzoic acid 
• 85-44-9 phthalic anhydride 

Downstream Products

• 101441-97-8 2-mesityl-4H-benzo[d][1,3]oxazin-4-one 
• 101596-89-8 3-mesitylisobenzofuran-1(3H)-one 
• 1393804-88-0 7-(2,4,6-trimethylphenyl)-2H-pyrimido[2,1-a]phthalazin-4(3H)-one 
• 1393805-13-4 6-(2,4,6-trimethylphenyl)-2-methylimidazo[2,1-a]phthalazin-3(2H)-one 
• 1393804-87-9 6-(2,4,6-trimethylphenyl)imidazo[2,1-a]phthalazin-3(2H)-one 
• 1393804-86-8 3-(4-(2,4,6-trimethylphenyl)phthalazin-1-ylamino)propanoic acid 
• 1393805-12-3 C₂₀H₂₁N₃O₂ 
• 1393804-85-7 2-(4-(2,4,6-trimethylphenyl)phthalazin-1-ylamino)acetic acid 
• 1393805-03-2 7-(2,4,6-trimethylphenyl)-3-methyl-2H-[1,2,4]triazino[3,4-a]phthalazine 
• 1393805-02-1 C₁₇H₁₈N₄ 
• 1393805-01-0 6-(2,4,6-trimethylphenyl)-tetrazolo[5,1-a]phthalazine 
• 1393805-00-9 7-(2,4,6-trimethylphenyl)-3-phenyl-2-thioxo-2,3-dihydro-[1,3,5]triazino[2,1-a]phthalazin-4-one 
• 1393804-98-2 7-(2,4,6-trimethylphenyl)-13H-phthalazino[2,1-a]quinazoline 
• 1393804-99-3 N-(4-chlorobenzylidene)-6-(2,4,6-trimethylphenyl)-[1,2,4]triazolo[3,4-a]phthalazin-3-amine 

Relevant academic research and scientific papers

Palladium-catalyzed chemoselective decarboxylative ortho acylation of benzoic acids with α-oxocarboxylic acids

Palladium-catalyzed chemoselective decarboxylative cross coupling of benzoic acids with α-oxocarboxylic acids was realized via an arene sp 2 C-H functionalization process. This work represents the first example of transition-metal-catalyzed cro

Synthesis and antimicrobial activity of some condensed [4-(2,4,6- trimethylphenyl)-1(2H)-oxo-phthalazin-2-yl]acetic acid hydrazide

Some new 1,2,4-triazolo-, 1,3,4-oxadiazolo-, 1,3,4-thiadiazol-, and pyrazolo-2,4,6-trimethylphenyl-1(2H)-oxo-phthalazine derivatives were synthesized and identified by IR, 1H NMR, 13C NMR, MS and elemental analysis. The new compounds were synthesized with the objective of studying their antimicrobial activity.

Synthesis and antimicrobial ealuation of some annelated phthalazine deriaties and acyclo C-nucleosides from 1-chloro-4-(2,4,6-trimethylphenyl) phthalazine precursor

A highly efficient and ersatile synthetic approach to the synthesis of annelated phthalazine deriaties iz. 1,2,4-triazolo[3,4-a]phthalazine 11a,b, 14, 18, 19a,b, 29-31, 33, 1,2,4-triazino[3,4-a]phthalazine 25a,b-28, 1,3,5-triazino[4,3-a]phthalazine 22, tetrazolo[5,1-a] phthalazine 23, imidazophthalazine 9a,b,15, and pyrimidinophthlazine 6, 10, 16, 17, 20 is presented. Moreoer, acyclo C -nucleoside and double headed acyclo C-nucleoside of 1,2,4-triazolo[3,4-a]phthalazine 12, 13 were obtained ia heterocyclization reaction of 1-chloro-4-(2,4,6-trimethylphenyl)phthalazine (4) with gluconic acid hydrazide and galactaric acid bis hydrazide, respectiely. The new compounds were synthesized with the objectie of studying their antimicrobial actiity. TUeBITAK.

An alternative route to syntheses of aryl keto acids in a chloroaluminate ionic liquid

The Lewis acidic 1-butyl-3-methylimidazolium chloroaluminate ionic liquid [bmim]Cl.AlCl3, N=0.67, is employed as a catalyst as well as the solvent for the quick and efficient syntheses of aryl keto acids by Friedel-Crafts acylation and aroylation of aromatic hydrocarbons using cyclic acid anhydrides.

Isoquinolinamine and phthalazinamine derivatives: corticotropin-releasing factor receptor CRF1 specific ligands

Disclosed are compounds that are highly selective partial agonists or antagonists at human CRF1receptors that are useful in the diagnosis and treatment of treating stress related disorders such as post traumatic stress disorder (PTSD) as well as depression, headache and anxiety. The compounds have the formula or the pharmaceutically acceptable salts thereof wherein Ar, R1, R2, R3, R4and W are various organic and inorganic substituents.

Isoquinolinamine and phthalazinamine derivatives: corticotropin-releasing factor receptor CRF1 specific ligands

Disclosed are compounds that are highly selective partial agonists or antagonists at human CRF1 receptors that are useful in the diagnosis and treatment of treating stress related disorders such as post traumatic stress disorder (PTSD) as well as depression, headache and anxiety. The compounds have the formula or the pharmaceutically acceptable salts thereof wherein Ar, R1, R2, R3, R4 and W are various organic and inorganic substituents.