2346-67-0

Basic information

• Product Name: 2-(2,4,6-TRIMETHYLBENZOYL)BENZOIC ACID
• Synonyms: 2-(2,4,6-TRIMETHYLBENZOYL)BENZOIC ACID;2-(mesitylcarbonyl)benzoic acid;2-[oxo-(2,4,6-trimethylphenyl)methyl]benzoic acid
• CAS NO: 2346-67-0
• Molecular Formula: C₁₇H₁₆O₃
• Molecular Weight: 268.32
• Mol File: 2346-67-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 433.2°Cat760mmHg
• Flash Point: 229.9°C
• Appearance: /
• Density: 1.172g/cm³
• Vapor Pressure: 2.84E-08mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: 2-(2,4,6-TRIMETHYLBENZOYL)BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4,6-TRIMETHYLBENZOYL)BENZOIC ACID(2346-67-0)
• EPA Substance Registry System: 2-(2,4,6-TRIMETHYLBENZOYL)BENZOIC ACID(2346-67-0)

Safety Data

• Hazardous Substances Data: 2346-67-0(Hazardous Substances Data)

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

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

Downstream Products

• 101596-89-8 3-mesitylisobenzofuran-1(3H)-one 
• 101441-97-8 2-mesityl-4H-benzo[d][1,3]oxazin-4-one 
• 19356-89-9 N-mesityl-phthalamic acid 
• 209416-34-2 4-(2,4,6-trimethylphenyl)-2,3-phthalazin-1-one 
• 33885-66-4 2-(2,4,6-Trimethyl-benzoyl)-benzoylchlorid 
• 209416-35-3 1-chloro-4-(2,4,6-trimethylphenyl)phthalazine 
• 95868-48-7 2,4,6-Trimethyl-2'-<2,4-dimethyl-benzoyl>-benzophenon 
• 7597-94-6 2-<2,4,6-Trimethyl-benzoyl>-benzophenon 
• 33885-59-5 2-(2,4,6-Trimethyl-benzoyl)-benzamid 
• 33885-64-2 2-(2.4.6-Trimethyl-benzoyl)-benzanilid 
• 1374218-43-5 4-mesityl-2-[(4-(4-nitrobenzylideneamino)-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)methyl]phthalazin-1(2H)-one 
• 1374218-20-8 2-(2-(3,5-dimethyl-1H-pyrazol-1-yl)-2-oxoethyl)-4-(2,4,6-trimethylphenyl)phthalazin-1(2H)-one 
• 1374218-21-9 1-[2-(4-mesityl-1-oxophthalazin-2(1H)-yl)acetyl]-pyrazolidine-3,5-dione 
• 1374218-22-0 5-methyl-3-oxo-2-[1(2H)-oxo-4-(2,4,6-trimethylphenyl)phthalazin-2-ylmethylcarbonyl]-3,4-dihydropyrazol 

Relevant articles and documents

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 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.

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.