76048-43-6

Basic information

• Product Name: Phenol, 2,4-dimethyl-, benzoate
• CAS NO: 76048-43-6
• Molecular Formula: C15H14O2
• Molecular Weight: 226.275
• Mol File: 76048-43-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phenol, 2,4-dimethyl-, benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2,4-dimethyl-, benzoate(76048-43-6)
• EPA Substance Registry System: Phenol, 2,4-dimethyl-, benzoate(76048-43-6)

Safety Data

• Hazardous Substances Data: 76048-43-6(Hazardous Substances Data)

Upstream product

• 93-97-0 benzoic acid anhydride 
• 105-67-9 2,4-Xylenol 
• 201230-82-2 carbon monoxide 
• 59-88-1 phenylhydrazine hydrochloride 
• 98-88-4 benzoyl chloride 

Downstream Products

• 76048-46-9 (2R^*,3S^*)-3'-chloro-5,7,dimethyl-3-phenylbenzofuran-2(3H)-spiro-1'(4'H)-naphthalen-4'-one 
• 76048-48-1 3',5,5',7-tetramethyl-3-phenylbenzofuran-2(3H)-spiro-1'-cyclohex-2',5'-dien-4'-one 
• 76048-44-7 bis<α-(2-hydroxy-3,5-dimethylphenyl)benzyl> ether 
• 76115-59-8 2-chloro-4-(2-hydroxy-3,5-dimethylphenyl)phenylmethyl-1-naphthol 
• 76115-58-7 2-<(4-hydroxy-3,5-dimethylphenyl)phenylmethyl>-4,6-dimethylphenol 
• 76048-42-5 (2-hydroxy-3,5-dimethylphenyl)phenylmethanol 
• 65-85-0 benzoic acid 
• 116544-61-7 [2,4-Dimethyl-6-(4-methyl-benzoyl)-phenoxy]-phenyl-acetic acid ethyl ester 
• 116544-71-9 [2,4-Dimethyl-6-(4-methyl-benzoyl)-phenoxy]-phenyl-acetic acid 
• 86914-85-4 2-Hydroxy-3,4',5-trimethyl-benzophenon 
• 55082-72-9 5,7-dimethyl-2-phenyl-3-p-tolyl-benzofuran 
• 16762-34-8 (2-hydroxy-3,5-dimethylphenyl)(phenyl)methanone 

Relevant articles and documents

Palladium-Catalyzed Oxidative Carbonylation of Aryl Hydrazines with CO and O2 at Atmospheric Pressure

Palladium-catalyzed aerobic oxidative aminocarbonylation and alkoxycarbonylation reactions with aryl hydrazines as coupling partners have been developed. The oxidative carbonylation of aryl hydrazines proceeded smoothly at atmospheric pressure CO, employi

Solid-Phase Benzoylation of Phenols and Alcohols in Microwave Reactor: An Ecofriendly Protocol

An efficient solid-phase benzoylation of phenols and alcohols was developed under microwave irradiation. A stoichiometric amount of benzoyl chloride was sufficient to carry out the reaction. This benzoylation features short reaction time, good yields, and easy workup procedures. Furthermore, the scope of the reaction was extended to prepare 3,5-dinitrobenzoyl derivatives of alcohols.