Ethyl 2-picolinate - ≥98%(GC) , CAS No.2524-52-9

CAS: 2524-52-9 Cat. No.: E133202 Peso molecular: 151.17 Beilstein Registry Number: 22(3/4)308 Número EC: 219-758-0

GRADE & PURITY ≥98%(GC)

Synonyms

Ethyl 2-picolinate, purum, >=99.0% (GC) | F0001-0852 | SCHEMBL126181 | STL558973 | STR01170 | UNII-RW5EU98AZQ | ETHYL PICOLINATE | FS-3192 | Ethyl2-picolinate | BCP25791 | Ethyl 2-picolinate | FT-0622196 | AM20050998 | Ethyl 2-picolinate, 99% | Picolinic

Storage

Room temperature

Shipped In

Normal

Descripción general

Ethyl picolinate is used in the preparation of 2-Aminodihydro[1,3]thiazines as BACE 2 inhibitors which is used in the treatment of diabetes. It is also used as pharmaceutical intermediate.

Specifications

Sinónimos

Ethyl 2-picolinate, purum, >=99.0% (GC) | F0001-0852 | SCHEMBL126181 | STL558973 | STR01170 | UNII-RW5EU98AZQ | ETHYL PICOLINATE | FS-3192 | Ethyl2-picolinate | BCP25791 | Ethyl 2-picolinate | FT-0622196 | AM20050998 | Ethyl 2-picolinate, 99% | Picolinic

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 504752822
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752822
• Sonrisas canónicas: CCOC(=O)C1=CC=CC=N1
• IUPAC Name: ethyl pyridine-2-carboxylate
• InChIKey: FQYYIPZPELSLDK-UHFFFAOYSA-N
• INCHI: 1S/C8H9NO2/c1-2-11-8(10)7-5-3-4-6-9-7/h3-6H,2H2,1H3
• Isómeros SMILES: CCOC(=O)C1=CC=CC=N1
• WGK Alemania: 3
• Peso molecular: 151.17
• Beilstein: 22(3/4)308
• Reaxy-Rn: 122485
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=122485&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Pyridines and derivatives
      • Subclass Pyridinecarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Pyridines and derivatives
• Subclass: Pyridinecarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridinecarboxylic acids
• Alternative Parents: Heteroaromatic compounds Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyridine carboxylic acid - Heteroaromatic compound - Carboxylic acid ester - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (no humanos)

Thrips tabaci (33 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Fully miscible in water.
• Índice de refracción: 1.511
• Punto de inflamación (°F): 224.6 °F
• Punto de inflamación (°C): 107°C(lit.)
• Punto de ebullición (°C): 240-241 °C
• Punto de fusión (°C): 2°C
• Peso molecular: 151.160 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 151.063 Da
• Monoisotopic Mass: 151.063 Da
• Topological Polar Surface Area: 39.200 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 136.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Xianglong Lei, Jun Tan, Pengfei Zhu, Chaozhen Zheng, Yao Liu, Le Zhang, Jun Luo, Jiugang Hu.  (2024)  Bidentate pyridine-pyrazole ligand-induced synergistic and antagonistic effects for selective separation of nickel from sulfuric acid medium.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.129188]

2. Xianglong Lei, Jun Tan, Yao Liu, Le Zhang, Pengfei Zhu, Jun Luo, Jiugang Hu.  (2025)  Dual Synergistic/Antagonistic Mechanism of Protonated-Amino Bidentate Ligand for Selective Separation of Nickel and Cobalt under High Acidity.  INORGANIC CHEMISTRY,      [PMID:41051885] [10.1021/acs.inorgchem.5c03830]