2,3-Dimethoxyphenol - ≥98% , CAS No.5150-42-5

CAS: 5150-42-5 Cat. No.: D473372 Formule: (CH₃O)₂C₆H₃OH Poids moléculaire: 154.16 Beilstein Registry Number: 1910050 Numéro CE: 225-922-2

GRADE & PURITY ≥98%

Synonyms

FT-0609683 | QSZCGGBDNYTQHH-UHFFFAOYSA-N | NSC 80659 | SY061558 | CHEBI:193967 | DTXSID10179832 | UNII-OW147I6C84 | 1-(phenanthren-2-yl)ethan-1-one | OW147I6C84 | 2,3-dim ethoxyphenol | Phenol, 2,3-dimethoxy- | NSC80659 | NSC-80659 | AKOS015888213 | 2,3-D

Storage

Argon charged,Room temperature

Shipped In

Normal

Vue d’ensemble

Description

2,3-Dimethoxyphenol is a plant-derived phenylpropanoid compound that is glycosidated to form glycoside compound.2,3-Dimethoxyphenol has been used to study the nitrosative deamination of DNA bases induced by reactive nitrogen species (RNS) while studying the cause of mutagenesis.

Specifications

Synonymes

FT-0609683 | QSZCGGBDNYTQHH-UHFFFAOYSA-N | NSC 80659 | SY061558 | CHEBI:193967 | DTXSID10179832 | UNII-OW147I6C84 | 1-(phenanthren-2-yl)ethan-1-one | OW147I6C84 | 2,3-dim ethoxyphenol | Phenol, 2,3-dimethoxy- | NSC80659 | NSC-80659 | AKOS015888213 | 2,3-D

Spécifications et pureté

≥98%

Conditions de stockage de stockage

Argon charged,Room temperature

Expédié en

Normal

Pureté

≥98%

Noms et identifiants

• Pubchem Sid: 488185626
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185626
• Sourires canoniques: COC1=CC=CC(=C1OC)O
• IUPAC Name: 2,3-dimethoxyphenol
• InChIKey: QSZCGGBDNYTQHH-UHFFFAOYSA-N
• INCHI: 1S/C8H10O3/c1-10-7-5-3-4-6(9)8(7)11-2/h3-5,9H,1-2H3
• Isomères SMILES: COC1=CC=CC(=C1OC)O
• WGK Allemagne: 3
• Poids moléculaire: 154.16
• Beilstein: 1910050
• Reaxy-Rn: 1910045
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1910045&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Phenols
      • Subclass Methoxyphenols

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Phenols
• Subclass: Methoxyphenols
• Intermediate Tree Nodes: Not available
• Direct Parent: Methoxyphenols
• Alternative Parents: Dimethoxybenzenes Phenoxy compounds Anisoles Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: O-dimethoxybenzene - Dimethoxybenzene - Methoxyphenol - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.
• 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

Propriétés chimiques et physiques

• Indice de réfraction: n20/D 1.539 (lit.)
• Point d'éclair (°F): 228.2 °F
• Point d'éclair (°C): 109 °C
• Point d'ébullition (°C): 233-234 °C (lit.)
• Poids moléculaire: 154.160 g/mol
• XLogP3: 1.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 154.063 Da
• Monoisotopic Mass: 154.063 Da
• Topological Polar Surface Area: 38.700 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 116.000
• 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

Références

1. Haoquan Guo, Xinyu Lu, Yue Yang, Jinhe Wei, Lizhi Wu, Li Tan, Yu Tang, Xiaoli Gu.  (2023)  Harvesting alkyl phenols from lignin monomers via selective hydrodeoxygenation under ambient pressure on Pd/α-MoC catalysts.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2023.113041]

2. Haoquan Guo, Jiwu Zhao, Yu Chen, Xinyu Lu, Yue Yang, Chenrong Ding, Lizhi Wu, Li Tan, Jinlin Long, Guohui Yang, Yu Tang, Noritatsu Tsubaki, Xiaoli Gu.  (2024)  Mechanistic Insights into Hydrodeoxygenation of Lignin Derivatives over Ni Single Atoms Supported on Mo2C.  ACS Catalysis,      [PMID:] [10.1021/acscatal.3c04555]

Foire aux questions

What is the purity of this product?

This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 5150-42-5, the molecular formula is (CH3O)2C6H3OH, and the molecular weight is 154.16 g/mol. InChIKey QSZCGGBDNYTQHH-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.