CAS 2454-37-7

3-(1-Hydroxyethyl)aniline

Description:

3-(1-Hydroxyethyl)aniline, also known by its CAS number 2454-37-7, is an organic compound that features both an aniline and a hydroxyethyl functional group. This compound is characterized by its aromatic amine structure, which consists of a benzene ring bonded to an amino group (-NH2) and a hydroxyethyl group (-CH(OH)CH3) at the meta position relative to the amino group. It is typically a colorless to light yellow liquid or solid, depending on its purity and form. The presence of the hydroxyethyl group enhances its solubility in polar solvents, making it more versatile in various chemical applications. 3-(1-Hydroxyethyl)aniline can participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic reactions, due to the reactivity of both the amino and hydroxy groups. This compound is often used in the synthesis of dyes, pharmaceuticals, and other organic compounds, highlighting its importance in industrial chemistry. Safety precautions should be taken when handling this substance, as it may pose health risks upon exposure.

Formula: C₈H₁₁NO

InChI: InChI=1S/C8H11NO/c1-6(10)7-3-2-4-8(9)5-7/h2-6,10H,9H2,1H3

InChI key: InChIKey=QPKNDHZQPGMLCJ-UHFFFAOYSA-N

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

Synonyms:

• (1R)-1-(3-aminophenyl)ethanol
• (1S)-1-(3-aminophenyl)ethanol
• (RS)-3-(1-Hydroxyethyl)aniline
• 1-(3-Aminophenyl)ethan-1-ol
• 1-(3-Aminophenyl)ethanol
• 3-Amino-alpha-methylbenzyl alcohol~3-Aminophenyl methyl carbinol~3-(alpha-Hydroxyethyl)aniline
• 3-Amino-α-methylbenzenemethanol
• 3-Amino-α-methylbenzyl alcohol
• Benzenemethanol, 3-amino-α-methyl-
• Benzyl alcohol, m-amino-α-methyl-
• NSC 62018
• NSC 8392
• [3-(1-Hydroxyethyl)phenyl]amine
• m-(1-Hydroxyethyl)aniline
• m-Amino-α-methylbenzyl alcohol

1-(3-Aminophenyl)ethanol, 98%

CAS: 2454-37-7

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₈H₁₁NO

Purity: 98%

Color and Shape: White to cream or pale yellow to pale brown, Crystals or crystalline powder

Molecular weight: 137.18

Ref: 02-L06513

Benzenemethanol, 3-amino-α-methyl-

CAS: 2454-37-7

Formula: C₈H₁₁NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 137.1790

Ref: IN-DA002OH5

Benzyl alcohol, m-amino-α-methyl-

CAS: 2454-37-7

Benzyl alcohol, m-amino-alpha-methyl- is a bioactive chemical.

Formula: C₈H₁₁NO

Color and Shape: Slightly Beige To Grey-Brown Powder Or Lumps

Molecular weight: 137.179

Ref: TM-T21106

1-(3-Aminophenyl)ethanol

CAS: 2454-37-7

1-(3-Aminophenyl)ethanol

Purity: 97%

Molecular weight: 137.18g/mol

Ref: 54-OR80327

1-(3-Aminophenyl)ethanol

CAS: 2454-37-7

Formula: C₈H₁₁NO

Purity: 95%

Color and Shape: Solid

Molecular weight: 137.182

Ref: 10-F208844

1-(3-Aminophenyl)ethanol

CAS: 2454-37-7

Formula: C₈H₁₁NO

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 137.18

Ref: 3B-A3221

3-(1-Hydroxyethyl)aniline

CAS: 2454-37-7

3-(1-Hydroxyethyl)aniline is a biomolecule that is created by the reaction of aniline and cyclohexanol. This reaction takes place in the presence of hydrochloric acid as a catalyst under hydrostatic pressure. The reaction products are characterized by their high surface area, which gives them excellent catalytic properties. 3-(1-Hydroxyethyl)aniline has been shown to be an efficient non-selective catalyst for reactions involving anilines and other aromatic compounds, such as styrene. It also has good selectivity for reactions with cyclohexanol over other alcohols, such as ethanol or methanol.

Formula: C₈H₁₁NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 137.18 g/mol

Ref: 3D-FA68011

1-(3-Aminophenyl)ethanol

CAS: 2454-37-7

Formula: C₈H₁₁NO

Molecular weight: 137.18

Ref: ST-EA-CP-R27029