1386393-98-1

Basic information

• Product Name: (E)-tert-butyl 4-(4-phenylbut-3-en-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
• CAS NO: 1386393-98-1
• Molecular Weight: 313.44
• Mol File: 1386393-98-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-tert-butyl 4-(4-phenylbut-3-en-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-tert-butyl 4-(4-phenylbut-3-en-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate(1386393-98-1)
• EPA Substance Registry System: (E)-tert-butyl 4-(4-phenylbut-3-en-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate(1386393-98-1)

Safety Data

• Hazardous Substances Data: 1386393-98-1(Hazardous Substances Data)

Upstream product

• 74-85-1 ethene 
• 6783-05-7 trans-2-phenylvinylboronic acid 
• 1386393-97-0 tert-butyl 4-[(1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl)oxy]-3,6-dihydropyridine-1(2H)-carboxylate 

Relevant articles and documents

Palladium-catalyzed 1,1-difunctionalization of ethylene

The 1,1-difunctionalization of ethylene, with aryl/vinyl/heteroaryl transmetalating agents and vinyl electrophiles, is reported. The reaction is high-yielding under a low pressure of ethylene, and regioselectivity is generally high for the 1,1-disubstituted product. The process is highlighted by the use of heteroaromatic cross-coupling reagents, which have not been competent reaction partners in previously reported efforts.