CAS 2549-14-6

(R)-(-)-2-Amino-1-phenylethanol

Description:

(R)-(-)-2-Amino-1-phenylethanol, also known as (R)-(-)-phenylalaninol, is an organic compound characterized by its chiral amine structure. It features an amino group (-NH2) and a hydroxyl group (-OH) attached to a two-carbon ethyl chain, with a phenyl group substituent on one of the carbons. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in water and various organic solvents, making it versatile in chemical reactions. The presence of both an amine and an alcohol functional group allows it to participate in hydrogen bonding, influencing its reactivity and interactions with other molecules. (R)-(-)-2-Amino-1-phenylethanol is often used in asymmetric synthesis and as a chiral auxiliary in the production of pharmaceuticals and fine chemicals. Its specific stereochemistry imparts unique properties that are valuable in enantioselective reactions, making it an important compound in the field of medicinal chemistry and organic synthesis.

Formula: C₈H₁₁NO

InChI: InChI=1/C8H11NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6,9H2/t8-/m0/s1

InChI key: InChIKey=ULSIYEODSMZIPX-QMMMGPOBSA-N

SMILES: [C@@H](CN)(O)C1=CC=CC=C1

Synonyms:

• ((R)-2-Hydroxy-2-phenylethyl)amine
• (-)-2-Amino-1-phenylethanol
• (-)-Phenylethanolamine
• (-)-α-(Aminomethyl)benzenemethanol
• (-)-β-Hydroxyphenethylamine
• (1R)-2-amino-1-phenylethanol
• (1S)-2-amino-1-phenylethanol
• (R)-(-)-1-Phenyl-2-aminoethanol
• (R)-α-(Aminomethyl)benzenemethanol
• (αR)-α-(Aminomethyl)benzenemethanol
• <span class="text-smallcaps">D</span>-(-)-β-Phenylethanolamine
• Benzenemethanol, α-(aminomethyl)-, (R)-
• Benzenemethanol, α-(aminomethyl)-, (αR)-
• Benzyl alcohol, α-(aminomethyl)-, (R)-(-)-
• D-(-)-β-Phenylethanolamine
• (R)-2-Amino-1-phenylethanol
• R-amino-1-phenylethanol
• (R)-ALPHA-(AMINOMETHYL)BENZYL ALCOHOL
• (r)-α-(aminomethyl)benzyl alcohol
• (r)-(-)-à-(aminomethyl)benzyl alcohol
• (R)-1-PHENYL-1-HYDROXY-2-AMINOETHANE
• R-2-AMINO-1-PHENYLETHANOL (R)-A-(AMINOMETHYL)BENZYL ALCOHOL
• (R)-(-)-2-AMINO-1-PHENYLETHANOL, 97%, EE 98%
• (R)-(+)-2-Phenylglycinol
• R-ALFUZOSIN
• RARECHEM AL BW 2319
• (1R)-1-Phenyl-2-aminoethanol

(R)-(-)-2-Amino-1-phenylethanol

CAS: 2549-14-6

Formula: C₈H₁₁NO

Purity: >96.0%(HPLC)

Color and Shape: White to Yellow to Orange powder to crystal

Molecular weight: 137.18

Ref: 3B-A2489

(R)-(-)-2-Amino-1-phenylethanol, 97%, ee 98%

CAS: 2549-14-6

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: powder, White

Molecular weight: 137.18

Ref: 02-L19403

(R)-2-Amino-1-phenylethanol

CAS: 2549-14-6

Formula: C₈H₁₁NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 137.1790

Ref: IN-DA003AYN

(1R)-(-)-2-Amino-1-phenylethan-1-ol

CAS: 2549-14-6

(1R)-(-)-2-Amino-1-phenylethan-1-ol

Formula: C₈H₁₁NO

Purity: 97%

Color and Shape: white crystalline solid

Molecular weight: 137.18g/mol

Ref: 54-OR3011

(R)-2-Amino-1-phenylethanol

CAS: 2549-14-6

(R)-2-Amino-1-phenylethanol is a molecule that has antimicrobial activity. It binds to the active site of bacterial enzymes, such as those involved in the synthesis of cell walls, and inhibits the growth of bacteria through competitive inhibition. This molecule also has a dihedral angle that is similar to that of other molecules with antibacterial activity. (R)-2-Amino-1-phenylethanol is an enantiomer, which means it can be synthesized from either (S)- or (R)-1-phenylethanol. The racemic form is more active than any individual enantiomer.

Formula: C₈H₁₁NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 137.18 g/mol

Ref: 3D-FA64085

(R)-2-Amino-1-phenylethanol

CAS: 2549-14-6

Formula: C₈H₁₁NO

Purity: 95%

Color and Shape: Solid

Molecular weight: 137.182

Ref: 10-F077860