2-(2-Aminoethyl)phenol - ≥98% , CAS No.2039-66-9

CAS: 2039-66-9 Cat. No.: A191948 Peso molecular: 137.18 Número EC: 218-016-3

GRADE & PURITY ≥98%

Synonyms

AKOS000155705 | SY040467 | A4439 | BDBM50240920 | o-hydroxyphenylethylamine | SCHEMBL1427697 | 2-(2-Hydroxyphenyl)Ethylamine | 2-(2-hydroxy-phenyl)-ethyl-amine | EN300-58297 | CHEBI:125487 | 2-tyramine | FT-0650908 | DTXSID50174326 | PHENOL, 2-(2-AMINOETH

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

AKOS000155705 | SY040467 | A4439 | BDBM50240920 | o-hydroxyphenylethylamine | SCHEMBL1427697 | 2-(2-Hydroxyphenyl)Ethylamine | 2-(2-hydroxy-phenyl)-ethyl-amine | EN300-58297 | CHEBI:125487 | 2-tyramine | FT-0650908 | DTXSID50174326 | PHENOL, 2-(2-AMINOETH

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

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: 504754876
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754876
• Sonrisas canónicas: C1=CC=C(C(=C1)CCN)O
• IUPAC Name: 2-(2-aminoethyl)phenol
• InChIKey: FMEVAQARAVDUNY-UHFFFAOYSA-N
• INCHI: 1S/C8H11NO/c9-6-5-7-3-1-2-4-8(7)10/h1-4,10H,5-6,9H2
• Isómeros SMILES: C1=CC=C(C(=C1)CCN)O
• Peso molecular: 137.18
• Reaxy-Rn: 1210320
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1210320&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Phenethylamines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenethylamines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenethylamines
• Alternative Parents: 2-arylethylamines Aralkylamines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Organopnictogen compounds Organooxygen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenethylamine - 2-arylethylamine - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Amine - Hydrocarbon derivative - Organopnictogen compound - Primary amine - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenethylamines. These are compounds containing a phenethylamine moiety, which consists of a phenyl group substituted at the second position by an ethan-1-amine.
• External Descriptors: a monoamine

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)

Taar1 Trace amine-associated receptor 1 (899 Activities)

Discover Target: Taar1

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

Mecanismos de acción

Propiedades químicas y físicas

• Peso molecular: 137.180 g/mol
• XLogP3: 1.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 137.084 Da
• Monoisotopic Mass: 137.084 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 95.300
• 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. Hongyu Chen, Jiayi Guo, Xinrui Sun, Peipei Tian, Wenping Zhu, Manman Sun, Zengchen Liu, Qingfeng Li, Yahong Chen.  (2026)  Analyte-guided precise regulation of gold nanoflower etching mechanism for enhanced dopamine selectivity via bisphenol-triggered Schiff base/Michael addition and intramolecular hydrogen bond synergy.  TALANTA,      [PMID:41558403] [10.1016/j.talanta.2026.129412]