1353682-15-1

Basic information

• Product Name: benzyl (R)-(1-phenylbuta-2,3-dien-1-yl)carbamate
• Synonyms: benzyl (R)-(1-phenylbuta-2,3-dien-1-yl)carbamate
• CAS NO: 1353682-15-1
• Molecular Weight: 279.338
• Mol File: 1353682-15-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl (R)-(1-phenylbuta-2,3-dien-1-yl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (R)-(1-phenylbuta-2,3-dien-1-yl)carbamate(1353682-15-1)
• EPA Substance Registry System: benzyl (R)-(1-phenylbuta-2,3-dien-1-yl)carbamate(1353682-15-1)

Safety Data

• Hazardous Substances Data: 1353682-15-1(Hazardous Substances Data)

Upstream product

• 935749-22-7 carbonic acid tert-butyl ester 1-phenyl-buta-2,3-dienyl ester 
• 621-84-1 O-benzyl carbamate 
• 865350-17-0 4,4,5,5-tetramethyl-2-(propa-1,2-dien-1-yl)-1,3,2-dioxaborolane 
• 136401-24-6 benzyl N-(1-methoxy-1-phenylmethyl)carbamate 

Relevant articles and documents

Ir-Catalyzed Enantioconvergent Synthesis of Diversely Protected Allenylic Amines Employing Ammonia Surrogates

The first iridium catalyzed, enantioconvergent amination of allenylic carbonates is reported. This process utilizes various commercially available carbamates and sulfonamides to generate allenylic amines including commonly employed protected groups (Boc, Fmoc, Cbz, Ts, Ns) in 62–82 % yield and 87–98 % ee. The products generated through this scalable procedure serve as effective linchpins for the rapid, enantiospecific synthesis of a wide range of complex structures.