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Ethyl 2-(2-chloropyridin-3-yl)acetate

  • CAS No. 164464-60-2

  • Cat. No. CS-0049541
  • Purity≥95%
  • MDL No.MFCD17214401

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

Ethyl 2-(2-chloropyridin-3-yl)acetate|CS-0049541

Structure of 164464-60-2

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General Information

  • CAS No. 164464-60-2
  • Cat. No. CS-0049541
  • Purity ≥95%
  • MDL No. MFCD17214401
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₀ClNO₂
  • Molecular Weight None
  • Synonym(s) Ethyl 2-chloropyridine-3-acetate
  • SMILES CCOC(=O)CC1=CC=CN=C1Cl

Description

Ethyl 2-(2-chloropyridin-3-yl)acetate features a chloropyridine moiety linked to an ethyl ester group, enabling direct incorporation into cross-coupling and functionalization reactions. This bench-stable reagent delivers efficient access to substituted pyridine derivatives under standard conditions.

Application

Ethyl 2-(2-chloropyridin-3-yl)acetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized pyridine derivatives. The molecule combines a reactive ester group with an electrophilic 2-chloropyridin-3-yl moiety, facilitating nucleophilic substitution and transition-metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it ideal for use in medicinal chemistry and process development workflows.

Safety Information

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Computational Chemistry Data

  • TPSA   39.19
  • LogP   1.8406
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   3

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