CAS 5344-90-1

2-Aminobenzyl alcohol

Description:

2-Aminobenzyl alcohol, with the CAS number 5344-90-1, is an organic compound characterized by the presence of both an amino group (-NH2) and a hydroxyl group (-OH) attached to a benzyl moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in water and organic solvents, making it versatile for various applications. The amino group contributes to its basicity, while the hydroxyl group provides potential for hydrogen bonding, influencing its reactivity and interactions with other substances. 2-Aminobenzyl alcohol is often utilized in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and as an intermediate in the synthesis of dyes and other chemical compounds. Its properties, such as melting point, boiling point, and specific reactivity, can vary based on the conditions and purity of the sample. Safety precautions should be observed when handling this compound, as it may pose health risks if ingested or inhaled.

Formula: C₇H₉NO

InChI: InChI=1S/C7H9NO/c8-7-4-2-1-3-6(7)5-9/h1-4,9H,5,8H2

InChI key: InChIKey=VYFOAVADNIHPTR-UHFFFAOYSA-N

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

Synonyms:

• (2-Aminophenyl)methanol
• (o-Aminophenyl)methanol
• 2-(Hydroxymethyl)aniline
• 2-Aminobenzenemethanol
• 2-Aminobenzylalcohol
• Benzenemethanol, 2-amino-
• Benzyl alcohol, o-amino-
• NSC 1173
• [2-(Hydroxymethyl)phenyl]amine
• o-(Hydroxymethyl)aniline
• o-Aminobenzyl alcohol

2-Aminobenzyl Alcohol

CAS: 5344-90-1

Formula: C₇H₉NO

Purity: >98.0%(GC)(T)

Color and Shape: White to Orange to Green powder to crystalline

Molecular weight: 123.16

Ref: 3B-A1000

2-Aminobenzyl alcohol, 98%

CAS: 5344-90-1

2-Aminobenzyl alcohol is oxidatively cyclised with an array of ketones in dioxane at 80C in the presence of a ruthenium catalyst and KOH to give corresponding quinolines. It undergoes oxidation catalyzed by heterotrimetallic RuMnMn species on the hydrotalcite surface in the presence of O2 to yield 2

Formula: C₇H₉NO

Purity: 98%

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

Molecular weight: 123.16

Ref: 02-A13180

2-Aminobenzyl Alcohol

CAS: 5344-90-1

Formula: C₇H₉NO

Purity: 98%

Color and Shape: Solid

Molecular weight: 123.1525

Ref: IN-DA003344

2-Aminobenzyl alcohol

CAS: 5344-90-1

2-Aminobenzyl alcohol

Formula: C₇H₉NO

Purity: ≥95%

Color and Shape: Light red. Solid

Molecular weight: 123.15246

Ref: 54-OR10943

2-Aminobenzyl alcohol

CAS: 5344-90-1

Formula: C₇H₉NO

Molecular weight: 123.16

Ref: 7W-GK6192

Tetracaine Impurity 4 (2-Aminobenzyl Alcohol)

CAS: 5344-90-1

Formula: C₇H₉NO

Color and Shape: Brown Solid

Molecular weight: 123.16

Ref: 4Z-T-1912

(2-Aminophenyl)methanol

Controlled Product

CAS: 5344-90-1

Formula: C₇H₉NO

Color and Shape: Neat

Molecular weight: 123.15

Ref: 86-MM0147.04

2-Aminobenzyl alcohol

CAS: 5344-90-1

(2-Aminophenyl)methanol

Formula: C₇H₉NO

Purity: 98%

Molecular weight: 123.15

Ref: IN-DG33991

Benzocaine EP Impurity B

CAS: 5344-90-1

Formula: C₇H₉NO

Molecular weight: 123.15

Ref: ST-EA-CP-B8002

2-Aminobenzyl Alcohol

Controlled Product

CAS: 5344-90-1

Applications 2-Aminobenzyl alcohol (cas# 5344-90-1) is a useful research chemical.

Formula: C₇H₉NO

Color and Shape: Neat

Molecular weight: 123.15

Ref: TR-A601828

2-Aminobenzyl alcohol

CAS: 5344-90-1

2-Aminobenzyl alcohol is a chaperone that binds to the polypeptide chain of proteins and prevents them from denaturation. It also has been shown to form hydrogen bonds with other molecules, such as chaperones, and to bind to copper ions. 2-Aminobenzyl alcohol can react with sodium carbonate in an alkaline solution to form 2-aminobenzaldehyde and sodium bicarbonate. The reaction mechanism is thought to involve the formation of a copper complex with x-ray diffraction data showing a new set of peaks at d = 1.81 Å corresponding to the Cu(II) ion coordinated by two amine groups on the benzyl alcohol ring. This compound also reacts with quinoline derivatives in the presence of hydrochloric acid or hydroxyl group in an aprotic solvent such as dimethylformamide (DMF) or acetonitrile (ACN) to produce mianserin hydro

Formula: C₇H₉NO

Purity: Min. 97.5%

Color and Shape: Off-White Powder

Molecular weight: 123.15 g/mol

Ref: 3D-FA64445

o-Amino-benzylalcohol

CAS: 5344-90-1

Formula: C₇H₉NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 123.155

Ref: 10-F036679