2-Pyridinemethanol - ≥98% , CAS No.586-98-1

CAS: 586-98-1 Cat. No.: P106578 Peso molecular: 109.13 Beilstein Registry Number: 107849 Número EC: 209-592-7

GRADE & PURITY ≥98%

Synonyms

2-Pyridine methanol | Pyridinemethanol | pyridine-methanol | 2-PYRIDINEMETHANOL | 2-pyridine-methanol | CHEBI:195070 | AE-641/00340018 | CCG-214048 | 2-(Hydroxymethyl)pyridine | 2-(hydroxymethyl)-pyridine | P0556 | Piconol | SCHEMBL29266 | 2-Pyridyl carbi

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Descripción general

Application

2-Pyridinemethanol is used as a pyridylalcohol with hypoglycemic activity.

Specifications

Sinónimos

2-Pyridine methanol | Pyridinemethanol | pyridine-methanol | 2-PYRIDINEMETHANOL | 2-pyridine-methanol | CHEBI:195070 | AE-641/00340018 | CCG-214048 | 2-(Hydroxymethyl)pyridine | 2-(hydroxymethyl)-pyridine | P0556 | Piconol | SCHEMBL29266 | 2-Pyridyl carbi

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504752135
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752135
• Sonrisas canónicas: C1=CC=NC(=C1)CO
• IUPAC Name: pyridin-2-ylmethanol
• InChIKey: SHNUBALDGXWUJI-UHFFFAOYSA-N
• INCHI: 1S/C6H7NO/c8-5-6-3-1-2-4-7-6/h1-4,8H,5H2
• Isómeros SMILES: C1=CC=NC(=C1)CO
• WGK Alemania: 3
• RTECS: UT4689000
• Peso molecular: 109.13
• Beilstein: 107849
• Reaxy-Rn: 107849
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=107849&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Pyridines and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Pyridines and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridines and derivatives
• Alternative Parents: Heteroaromatic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
• 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)

Galc Galactocerebrosidase (11 Activities)

Discover Target: Galc

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

Rattus norvegicus (775804 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.
• Sensibilidad: Light sensitive；Hygroscopic；Air sensitive
• Punto de inflamación (°F): 242.6 °F
• Punto de inflamación (°C): 117 °C
• Punto de ebullición (°C): 112°C/15mmHg
• Punto de fusión (°C): -6 to -5°
• Peso molecular: 109.130 g/mol
• XLogP3: 0.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 109.053 Da
• Monoisotopic Mass: 109.053 Da
• Topological Polar Surface Area: 33.100 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 65.500
• 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. An Zhidong, Yang Piaoping, Duan Delong, Li Jiang, Wan Tong, Kong Yue, Caratzoulas Stavros, Xiang Shuting, Liu Jiaxing, Huang Lei, Frenkel Anatoly I., Jiang Yuan-Ye, Long Ran, Li Zhenxing, Vlachos Dionisios G..  (2023)  Highly active, ultra-low loading single-atom iron catalysts for catalytic transfer hydrogenation.  Nature Communications,  14  (1): (1-12).  [PMID:37863924] [10.1038/s41467-023-42337-9]

2. Lei Yuan, Hongshuai Gao, Haiyan Jiang, Shaojuan Zeng, Tao Li, Baozeng Ren, Xiangping Zhang.  (2020)  Experimental and thermodynamic analysis of NH3 absorption in dual-functionalized pyridinium-based ionic liquids.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2020.114601]

3. Zhang Guofu, Zhang Guihua, Lei Jie, Li Shasha, Xu Shengjun, Ding Chengrong, Shan Shang.  (2016)  Aerobic alcohol ammoxidation catalyzed by copper(I)/amino acid: a scalable protocol to nitriles.  CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,  32  (4): (586-593).  [PMID:] [10.1007/s40242-016-6067-9]

4. Wenhua Xue, Jian Ye, Zhi Zhu, Reeti Kumar, Jun Zhao.  (2024)  Harnessing trace water for enhanced photocatalytic oxidation of biomass-derived alcohols to aldehydes.  Energy & Environmental Science,      [PMID:] [10.1039/D4EE02301C]