205433-80-3

Basic information

• Product Name: 2,6-Diallyl-4-benzyloxy-phenol
• Synonyms: 2,6-Diallyl-4-benzyloxy-phenol
• CAS NO: 205433-80-3
• Molecular Weight: 280.367
• Mol File: 205433-80-3.mol

Chemical Properties

• CAS DataBase Reference: 2,6-Diallyl-4-benzyloxy-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Diallyl-4-benzyloxy-phenol(205433-80-3)
• EPA Substance Registry System: 2,6-Diallyl-4-benzyloxy-phenol(205433-80-3)

Safety Data

• Hazardous Substances Data: 205433-80-3(Hazardous Substances Data)

Upstream product

• 205433-79-0 2-Allyl-1-allyloxy-4-benzyloxy-benzene 

Downstream Products

• 403612-30-6 4-[2-(2,6-Diallyl-4-benzyloxy-phenoxy)-ethyl]-5-methyl-2-phenyl-oxazole 
• 403612-24-8 (2,6-Diallyl-4-benzyloxy-phenoxy)-acetic Acid Ethyl Ester 
• 205433-81-4 2,6-diallyl-4-benzyloxy-1-methoxybenzene 

Relevant articles and documents

Oxazolyl-aryloxyacetic acid derivatives and their use as ppar agonists

Compounds represented by the following (I), and pharmaceutically acceptable salts, solvates and hydrates thereof, wherein R1 is an unsubstituted or substituted aryl, heteroaryl, cycloalkyl, aryl-alkyl, heteroaryl-alkyl or cycloalkyl-alkyl, R2 is H, alkyl or haloalkyl, the polymethylene chain (II), is saturated or may contain a carbon-carbon double bond, while n is 2, 3, 4, W is O or S, Y is an unsubsituted or substituted phenylene, naphthylene or 1, 2, 3, 4 tetrahydronaphthylene, R3 is H, alkyl or haloalkyl. R4 is H, alkyl, haloalkyl or a substituted or unsubstituted benzyl, are useful for modulating a peroxisome proliferator activated receptor, particularly in the treatment of diabetes mellitus.

Photochemistry of Substituted 4,4-Dimethoxy-2,5-Cyclohexadienones

4,4-Dimethoxy-2,5-cyclohexadienones 9-14 were prepared from the corresponding hydroquinone monomethyl ethers by oxidation with thallium trinitrate in methanol. Irradiation of solutions of 9-13 in methanol with a broad band of UV light centered at 350 nm in a Rayonet reactor afforded 2-cyclopentenone derivatives 15-19 in moderate to excellent yields, whereas irradiation of 14 in methanol gave phenol 8 along with other unidentified products. Irradiation of 11-14 in benzene yielded substituted phenols. The plausible reaction pathways for the product formation are discussed.