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Methyl 6-amino-5-fluoronicotinate

  • CAS No. 1256792-42-3

  • Cat. No. CS-0149402
  • Molecule weightNone
  • Purity≥97%
  • MDL No.MFCD18250741

*For research and further manufacturing use only, not for direct human use.

Methyl 6-amino-5-fluoronicotinate|CS-0149402

Structure of 1256792-42-3

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General Information

  • CAS No. 1256792-42-3
  • Cat. No. CS-0149402
  • Purity ≥97%
  • MDL No. MFCD18250741
  • Storage RT, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₇FN₂O₂
  • Molecular Weight None
  • Synonym(s) methyl 6-amino-5-fluoropyridine-3-carboxylate
  • SMILES O=C(C1=CC(F)=C(N)N=C1)OC

Description

Methyl 6-amino-5-fluoronicotinate features a fluorinated pyridine core with strategically positioned amino and ester functionalities. This electron-deficient heterocycle integrates readily into medicinal chemistry scaffolds, offering enhanced metabolic stability and targeted bioavailability in kinase inhibitor development.

Application

Methyl 6-amino-5-fluoronicotinate serves as a versatile building block in medicinal chemistry, enabling direct access to fluorinated pyridine scaffolds common in kinase inhibitors and CNS-targeted therapeutics. The amino and ester functionalities offer orthogonal reactivity—facilitating amide coupling, electrophilic substitution, or directed metalation—while the methyl ester supports facile hydrolysis or transformation into carboxylic acid derivatives. Bench-stable and readily purified by recrystallization, it functions efficiently in standard coupling protocols and multistep syntheses.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   65.21
  • LogP   0.5895
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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