1644382-37-5

Basic information

• Product Name: C₁₀H₁₂FN
• Synonyms: C₁₀H₁₂FN
• CAS NO: 1644382-37-5
• Molecular Weight: 165.21
• Mol File: 1644382-37-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₀H₁₂FN(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₀H₁₂FN(1644382-37-5)
• EPA Substance Registry System: C₁₀H₁₂FN(1644382-37-5)

Safety Data

• Hazardous Substances Data: 1644382-37-5(Hazardous Substances Data)

Upstream product

• 1003-98-1 2-bromo-4-fluoroaniline 
• 67883-62-9 2-methylallyltributyltin 
• 61272-76-2 4-fluoro-2-iodoaniline 
• 1441421-59-5 N,N-diallyl-4-fluoro-2-iodoaniline 
• 769-42-6 1,3-dimethylbarbituric acid 
• 1627210-89-2 C₁₆H₂₀FN 

Downstream Products

• 1640995-86-3 C₁₇⁽¹³⁾CH₁₈N₂O₂S 
• 1627210-70-1 C₁₈H₁₇FN₂O₂S 
• 1627210-58-5 C₁₈H₁₇FN₂O₂S 
• 1627210-94-9 C₁₇H₁₈FNO₂S 

Relevant articles and documents

Palladium(II)-catalyzed intramolecular tandem aminoalkylation via divergent C(sp3)-H functionalization

(Chemical Equation Presented) We have developed a Pd(II)-catalyzed oxidative tandem aminoalkylation via divergent C(sp3)-H functionalization, a ffording three- and five-membered-ring fused indolines in good yields under two optimized conditions, respectively. The mechanism studies have indicated that the benzylic C - H cleavage involved in the former transformation is the rate-determining step, while the cleavage of amide α-C - H in the latter is not. This is the first example of a Pd-catalyzed tandem reaction involving C(sp3)-H activation without the employment of prefunctionalized reagents (e.g., halogenated and boron reagents) and directing groups, representing a green and economic protocol for the construction of N-containing heterocycles.