CAS 104-10-9

2-(4-Aminofenil)etanol

Descripción:

2-(4-Aminofenil)etanol, también conocido como para-aminofeniletilanol, es un compuesto orgánico caracterizado por la presencia de un grupo amino (-NH2) y un grupo hidroxilo (-OH) unidos a un anillo fenílico. Este compuesto presenta una cadena etílica de dos carbonos que une el grupo fenílico sustituido por amino al grupo hidroxilo. Típicamente es un sólido blanco a blanco sucio a temperatura ambiente y es soluble en agua y disolventes orgánicos debido a sus grupos funcionales polares. La presencia del grupo amino le confiere propiedades básicas, permitiéndole participar en diversas reacciones químicas, incluyendo acilación y alquilación. 2-(4-Aminofenil)etanol es de interés en la química medicinal y puede servir como precursor en la síntesis de fármacos, particularmente en el desarrollo de analgésicos y agentes antiinflamatorios. Además, puede ser utilizado en la fabricación de colorantes y como reactivo en la síntesis orgánica. Se deben observar precauciones de seguridad al manipular este compuesto, ya que puede representar riesgos para la salud al estar expuesto.

Fórmula: C₈H₁₁NO

InChI: InChI=1S/C8H11NO/c9-8-3-1-7(2-4-8)5-6-10/h1-4,10H,5-6,9H2

Clave InChI: InChIKey=QXHDYMUPPXAMPQ-UHFFFAOYSA-N

SMILES: C(CO)C1=CC=C(N)C=C1

Sinónimos:

• 2-(4-Amino-phenyl)ethanol
• 2-(4-Aminophenyl) ethanol
• 2-(4-Aminophenyl)-1-ethanol
• 2-(4-Aminophenyl)ethyl alcohol
• 2-(p-Aminophenyl)ethanol
• 4-(2-Hydroxyethyl)aniline
• 4-(2-Hydroxyethyl)phenylamine
• 4-Amino Phenethyl Alcohol
• 4-Aminobenzeneethanol
• 4-Aminophenethyl alcohol
• Benzeneethanol, 4-amino-
• NSC 409780
• P-Amino Phenethyl Alcohol
• P-Aminophenethyl Alcohol
• Phenethyl alcohol, p-amino-

2-(4-Aminophenyl)ethanol, 97%

CAS: 104-10-9

2-(4-Aminophenyl)ethanol is used as nonsymmetric monomer in the preparation of ordered [head-to-head (H-H) or tail-to-tail (T-T)] poly(amide-ester), in the synthesis of 4-aminostyrene and in functionalization of graphene nanoplatelets. This Thermo Scientific Chemicals brand product was originally

Fórmula: C₈H₁₁NO

Pureza: 97%

Forma y color: Pale cream to cream to yellow to brown, Crystals or powder or crystalline powder or lumps or granules

Peso molecular: 137.18

Ref: 02-L15223

2-(4-Aminophenyl)ethanol

CAS: 104-10-9

Fórmula: C₈H₁₁NO

Pureza: 95%

Forma y color: Solid

Peso molecular: 137.1790

Ref: IN-DA00380M

4-Aminophenethyl alcohol

CAS: 104-10-9

Fórmula: C₈H₁₁NO

Peso molecular: 137.18

Ref: 7W-GK6574

4-Aminophenethyl alcohol

CAS: 104-10-9

4-Aminophenethyl alcohol

Fórmula: C₈H₁₁NO

Pureza: ≥95%

Forma y color: brown crystalline powder

Peso molecular: 137.17903g/mol

Ref: 54-OR0014

2-(4-Aminophenyl)ethanol

CAS: 104-10-9

Fórmula: C₈H₁₁NO

Pureza: >98.0%(GC)(T)

Forma y color: White to Light yellow to Light orange powder to crystal

Peso molecular: 137.18

Ref: 3B-A0394

4-Aminophenethyl alcohol

CAS: 104-10-9

Fórmula: C₈H₁₁NO

Pureza: 95%

Forma y color: Solid, Chunks or Crystalline Powder

Peso molecular: 137.182

Ref: 10-F005442

4-Aminophenethyl Alcohol

Producto controlado

CAS: 104-10-9

Applications 4-Aminophenethyl Alcohol, is a building block that can be used in the synthesis of various compounds, such as in synthesis of 4-aminostyrene, and in functionalization of graphene nanoplatelets.
References Li L, et al.Polymer Journal 33(4), 364-370; Hagiwara T, et al. Macromolecules 24(26), 6856-6858, (1991);

Fórmula: C₈H₁₁NO

Forma y color: Neat

Peso molecular: 137.18

Ref: TR-A585045

2-(4-Aminophenyl)ethanol

CAS: 104-10-9

Fórmula: C₈H₁₁NO

Peso molecular: 137.18

Ref: ST-EA-CP-G91005

4-Aminophenethyl alcohol

CAS: 104-10-9

4-Aminophenethyl alcohol is a monosubstituted, basic compound that is used in the laboratory as a cell culture medium supplement to promote growth of fibroblasts. This compound has been shown to stimulate human intestinal cells and human peripheral blood mononuclear cells. 4-Aminophenethyl alcohol acts as a hydroxyl group donor, which may be due to its ability to form hydrogen ions when reacted with sodium hydroxide solution. The reaction of this compound with diazonium salt produces an intermediate, which can be hydrolyzed by the addition of sodium hydroxide solution. The resultant chloride ion reacts with the aminophenethyldihydroxylamine (APDA) moiety to produce APDCl. This product has been shown to increase the population growth rate of fibroblasts in culture by causing DNA synthesis and protein synthesis. Linear regression analysis revealed that there was no statistically significant difference between the control and experimental groups for either DNA

Fórmula: C₈H₁₁NO

Pureza: Min. 95%

Peso molecular: 137.18 g/mol

Ref: 3D-FA70793