917507-05-2

Basic information

• Product Name: 3-Buten-2-ol, 2-methyl-4-(2-methylphenyl)-, (3E)-
• CAS NO: 917507-05-2
• Molecular Formula: C12H16O
• Molecular Weight: 176.258
• Mol File: 917507-05-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Buten-2-ol, 2-methyl-4-(2-methylphenyl)-, (3E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Buten-2-ol, 2-methyl-4-(2-methylphenyl)-, (3E)-(917507-05-2)
• EPA Substance Registry System: 3-Buten-2-ol, 2-methyl-4-(2-methylphenyl)-, (3E)-(917507-05-2)

Safety Data

• Hazardous Substances Data: 917507-05-2(Hazardous Substances Data)

Upstream product

• 34222-71-4 1-methyl-2-((E)-2-nitro-vinyl)-benzene 
• 67-63-0 isopropyl alcohol 
• 115-19-5 2-methyl-but-3-yn-2-ol 
• 615-37-2 ortho-methylphenyl iodide 
• 40888-14-0 2-methyl-4-(2-methylphenyl)-3-butyn-2-ol 

Downstream Products

• 917507-06-3 (3E)-2-methoxy-2-methyl-4-(2-methylphenyl)-3-butene 

Relevant articles and documents

Copper-Catalyzed Alkenylation of Alcohols with β-Nitrostyrenes via a Radical Addition-Elimination Process

A new method for the preparation of allylic alcohol derivatives has been developed via a radical mechanism using DTBP as the radical initiator promoted by copper salt. The C(sp3)-H bond in various alcohols, toluene derivatives, and alkanes were successfully converted into C-C bonds to yield the desired products in moderate to good yields.

Vinyl hydrogen more reactive than benzyl hydrogen toward base in significantly twisted styrenes

The novel example of vinyl hydrogen more reactive than benzylic hydrogen was found by treatment of a twisted styrene derivative with a strong base followed by D2O quenching. The characteristic nature of the vinyl hydrogen, which is activated by