17100-43-5

Basic information

• Product Name: (4-(but-3-en-1-yl)phenyl)methanol
• Synonyms: (4-(but-3-en-1-yl)phenyl)methanol
• CAS NO: 17100-43-5
• Molecular Weight: 162.232
• Mol File: 17100-43-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-(but-3-en-1-yl)phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(but-3-en-1-yl)phenyl)methanol(17100-43-5)
• EPA Substance Registry System: (4-(but-3-en-1-yl)phenyl)methanol(17100-43-5)

Safety Data

• Hazardous Substances Data: 17100-43-5(Hazardous Substances Data)

Upstream product

• 71831-21-5 4-(bromomethyl)benzyl alcohol 
• 106-95-6 allyl bromide 
• 107-05-1 3-chloroprop-1-ene 
• 137658-83-4 4-(3-butenyl)-benzaldehyde 
• 15451-32-8 1-(3-butenyl)-4-bromobenzene 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 50-00-0 formaldehyd 
• 3047-24-3 4-(p-chlorophenyl)-1-butene 

Downstream Products

• 38632-66-5 4-(4-hydroxymethylphenyl)butan-1-ol 
• 454678-90-1 (E)-(4-(but-1-en-1-yl)phenyl)methanol 
• 53332-82-4 -<4-(4-chlormethylphenyl)butyl>methylsilan 
• 49853-97-6 -<4-(4-chlormethylphenyl)butyl>dimethylsilan 
• 53332-81-3 4-(4-Chlormethylphenyl)-1-buten 

Relevant articles and documents

Chemo-, regio-, and stereoselective iron-catalysed hydroboration of alkenes and alkynes

The highly chemo-, regio-, and stereoselective synthesis of alkyl- and vinyl boronic esters with good functional group tolerance has been developed using in situ activation of a bench-stable iron(ii) pre-catalyst and pinacolborane (16 examples, 45-95% yield, TOF up to 30000 mol h-1). The first iron-catalysed alkene hydrogermylation is also reported.

Palladium-Catalyzed Electrochemical Allylic Alkylation between Alkyl and Allylic Halides in Aqueous Solution

A new route for the direct cross-coupling of alkyl and allylic halides using electrochemical technique has been developed in aqueous media under air. Catalyzed by Pd(OAc)2, the Zn-mediated allylic alkylations proceed smoothly between a full range of alkyl halides (primary, secondary, and tertiary) and substituted allylic halides. Protection-deprotection of acidic hydrogen in the substrates is avoided.