Sodium phenoxide - ≥98% , CAS No.139-02-6

CAS: 139-02-6 Cat. No.: S190796 Formula: C₆H₅NaO Peso molecolare: 116.09 Numero EC: 205-347-3

GRADE & PURITY ≥98%

Synonyms

Sodium phenoxide|139-02-6|SODIUM PHENOLATE|Phenolate sodium|sodium benzenolate|Sodium phenate|Phenol, sodium salt|Sodium carbolate|Phenol sodium salt|sodium;phenoxide|Phenolate sodium [USAN]|naoph|Phenol, sodium salt (1:1)|DTXSID4027072|CHEBI:52476|4NC0T5

Storage

Room temperature,Argon charged

Shipped In

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Panoramica

Sodium phenoxide is used as a precursor to aryl ethers and involved in the preparation of phenyl ethers and metal phenolates. It serves as an antiseptic and used in organic synthesis.

Specifications

Sinonimi

Sodium phenoxide | 139-02-6 | SODIUM PHENOLATE | Phenolate sodium | sodium benzenolate | Sodium phenate | Phenol, sodium salt | Sodium carbolate | Phenol sodium salt | sodium;phenoxide | Phenolate sodium [USAN] | naoph | Phenol, sodium salt (1:1) | DTXSID4027072 | CHEBI:52476 | 4NC0T5

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

FedEx DG Service

Nota

Incompatible with oxidizing agents.

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 528775387
• Sorrisi canonici: C1=CC=C(C=C1)[O-].[Na+]
• IUPAC Name: sodium;phenoxide
• InChIKey: NESLWCLHZZISNB-UHFFFAOYSA-M
• INCHI: 1S/C6H6O.Na/c7-6-4-2-1-3-5-6;/h1-5,7H;/q;+1/p-1
• Isomeri SMILES: C1=CC=C(C=C1)[O-].[Na+]
• CAS alternativo: 156150-40-2
• Numero UN: 2905
• Gruppo di imballaggio: III
• Peso molecolare: 116.09

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Phenoxides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Phenoxides
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenoxides
• Alternative Parents: Organooxygen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxide - Organic alkali metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phenoxides. These are salts or analogous metal derivatives of phenols.
• External Descriptors: phenolate

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

Proprietà chimiche e fisiche

• Solubilità: Very soluble in water, soluble in alcoholSoluble in water, acetone and alcohol.
• Sensibilità: Air Sensitive；Moisture sensitive
• Punto di fusione (°C): >300°C
• Peso molecolare: 116.090 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 116.024 Da
• Monoisotopic Mass: 116.024 Da
• Topological Polar Surface Area: 23.100 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 50.500
• 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: 2

XLogP3

Riferimenti

1. Zifeng Yang, Lei Liu, Hongzhe An, Chenhao Li, Zhencai Zhang, Wenjuan Fang, Fei Xu, Suojiang Zhang.  (2020)  Cost-Effective Synthesis of High Molecular Weight Biobased Polycarbonate via Melt Polymerization of Isosorbide and Dimethyl Carbonate.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.0c00430]

2. Xianghe Meng, Lei Li, Qin Ye, Frederik van de Voort.  (2015)  Fourier Transform Infrared (FTIR) Spectroscopy as a Utilitarian Tool for the Routine Determination of Acidity in Ester-Based Oils.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:26321291] [10.1021/acs.jafc.5b02738]