1610455-66-7

Basic information

• Product Name: C₁₃H₁₅ClO₂
• CAS NO: 1610455-66-7
• Molecular Weight: 238.714
• Mol File: 1610455-66-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₃H₁₅ClO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₃H₁₅ClO₂(1610455-66-7)
• EPA Substance Registry System: C₁₃H₁₅ClO₂(1610455-66-7)

Safety Data

• Hazardous Substances Data: 1610455-66-7(Hazardous Substances Data)

Upstream product

• 1387563-26-9 C₁₃H₁₆O₃ 
• 114671-88-4 C₁₅H₂₀O₃ 
• 1195-81-9 ethyl 1-(hydroxymethyl)cyclobutanecarboxylate 
• 3779-29-1 diethyl cyclobutane-1,1-dicarboxylate 

Downstream Products

• 1610455-69-0 1-((benzyloxy)methyl)-N-(4-cyano-2,3,5,6-tetrafluorophenyl)cyclobutanecarboxamide 
• 1610456-25-1 1-((benzyloxy)methyl)-N-(4-cyano-2,3,5,6-tetrafluorophenyl)-2-phenylcyclobutanecarboxamide 

Relevant articles and documents

Pd(II)-Catalyzed Enantioselective C(sp3)-H Borylation

Pd(II)-catalyzed enantioselective borylation of C(sp3)-H bonds has been realized for the first time using chiral acetyl-protected aminomethyl oxazoline ligands. This reaction is compatible with carbocyclic amides containing α-tertiary as well as α-quaternary carbon centers. The chiral β-borylated amides are useful synthons for the synthesis of chiral β-hydroxylated, β-fluorinated, and β-arylated carboxylic acids.