1613507-32-6

Basic information

• Product Name: (R,E)-3-(4-phenylbut-3-en-2-yl)benzonitrile
• Synonyms: (R,E)-3-(4-phenylbut-3-en-2-yl)benzonitrile
• CAS NO: 1613507-32-6
• Molecular Weight: 233.313
• Mol File: 1613507-32-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R,E)-3-(4-phenylbut-3-en-2-yl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (R,E)-3-(4-phenylbut-3-en-2-yl)benzonitrile(1613507-32-6)
• EPA Substance Registry System: (R,E)-3-(4-phenylbut-3-en-2-yl)benzonitrile(1613507-32-6)

Safety Data

• Hazardous Substances Data: 1613507-32-6(Hazardous Substances Data)

Upstream product

• 1393640-41-9 C₂₁H₁₂B₃N₃O₃ 
• 326804-25-5 (S)-4-phenylbutan-2-yl pivalate 

Downstream Products

• 22161-81-5 S-ketoprofen 
• 1613507-33-7 C₂₃H₂₀O 

Relevant articles and documents

Enantiospecific, nickel-catalyzed cross-couplings of allylic pivalates and arylboroxines

We have developed an enantiospecific, nickel-catalyzed cross-coupling of unsymmetric 1,3-disubstituted allylic pivalates with arylboroxines. The success of this reaction relies on the use of BnPPh2 as a supporting ligand for the nickel(0) catalyst and NaOMe as a base. This method shows excellent functional group tolerance and broad scope in both the allylic pivalate and arylboroxine, enabling the preparation of 1,3-diaryl allylic products in high yields with excellent levels of regioselectivity and stereochemical fidelity.