39094-08-1

Basic information

• Product Name: 1-Naphthaleneacetic acid, a-phenyl-
• CAS NO: 39094-08-1
• Molecular Formula: C18H14O2
• Molecular Weight: 262.308
• Mol File: 39094-08-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Naphthaleneacetic acid, a-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthaleneacetic acid, a-phenyl-(39094-08-1)
• EPA Substance Registry System: 1-Naphthaleneacetic acid, a-phenyl-(39094-08-1)

Safety Data

• Hazardous Substances Data: 39094-08-1(Hazardous Substances Data)

Upstream product

• 103-82-2 phenylacetic acid 
• 90-11-9 1-Bromonaphthalene 
• 703-55-9 1-naphthylmagnesiumbromide 
• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 91-20-3 naphthalene 
• 124-38-9 carbon dioxide 
• 611-45-0 1-Benzyl-naphthalene 
• 6309-40-6 (+/-)-hydroxy-phenyl-(naphthyl-⁽¹⁾)-acetic acid 
• 6974-51-2 2-(naphthalen-1-yl)-2-phenylacetonitrile 
• 532-28-5 (RS)-mandelonitrile 

Downstream Products

• 506441-06-1 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (2R)-2-(1-naphthyl)-2-phenylethanoate 
• 238-84-6 benzo[a]fluorene 
• 858437-77-1 [1]naphthyl-phenyl-acetyl chloride 

Relevant articles and documents

Palladium-Catalyzed ?±-Arylation of Aryl Acetic Acid Derivatives via Dienolate Intermediates with Aryl Chlorides and Bromides

To date, examples of ?±-arylation of carboxylic acids remain scarce. Using a deprotonative cross-coupling process (DCCP), a method for palladium-catalyzed ?3-arylation of aryl acetic acids with aryl halides has been developed. This protocol is applicable to a wide range of aryl bromides and chlorides. A procedure for the palladium-catalyzed ?±-arylation of styryl acetic acids is also described.