1353864-35-3

Basic information

• Product Name: C₁₅H₁₉NO₄
• Synonyms: C₁₅H₁₉NO₄
• CAS NO: 1353864-35-3
• Molecular Weight: 277.32
• Mol File: 1353864-35-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₅H₁₉NO₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₁₉NO₄(1353864-35-3)
• EPA Substance Registry System: C₁₅H₁₉NO₄(1353864-35-3)

Safety Data

• Hazardous Substances Data: 1353864-35-3(Hazardous Substances Data)

Upstream product

• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 1353864-33-1 C₂₀H₃₂N₂O₄Si 
• 1353864-31-9 C₂₀H₃₄N₂O₄Si 

Downstream Products

• 1353864-37-5 N-Boc-trans-4-methyl-L-proline benzyl ester 
• 364750-80-1 (2S,4R)-1-[(tert-butoxy)carbonyl]-4-methylpyrrolidine-2-carboxylic acid 
• 138512-74-0 1-tert-butyl 2-methyl (2S,4R)-4-methylpyrrolidine-1,2-dicarboxylate 

Relevant articles and documents

Highly efficient syntheses of azetidines, pyrrolidines, and indolines via palladium catalyzed intramolecular amination of C(sp3)-H and C(sp2)-H bonds at γ and δ positions

Efficient methods have been developed to synthesize azetidine, pyrrolidine, and indoline compounds via palladium-catalyzed intramolecular amination of C-H bonds at the γ and δ positions of picolinamide (PA) protected amine substrates. These methods feature relatively a low catalyst loading, use of inexpensive reagents, and convenient operating conditions. Their selectivities are predictable. These methods highlight the use of unactivated C-H bond, especially the C(sp3)-H bond of methyl groups, as functional groups in organic synthesis.