CAS 46032-98-8

(1R,2R)-2-Amino-1-phenyl-1,3-propanediol

Description:

(1R,2R)-2-Amino-1-phenyl-1,3-propanediol, with the CAS number 46032-98-8, is an organic compound characterized by its chiral structure, which includes an amino group and two hydroxyl groups attached to a propanediol backbone. This compound is typically found in a solid state at room temperature and is soluble in polar solvents due to the presence of hydroxyl groups, which can engage in hydrogen bonding. The phenyl group contributes to its hydrophobic character, influencing its overall solubility and reactivity. As an amino alcohol, it can participate in various chemical reactions, including those typical of amines and alcohols, making it a valuable intermediate in organic synthesis. Its stereochemistry is significant, as the (1R,2R) configuration can affect its biological activity and interactions with other molecules. This compound may be utilized in pharmaceutical applications, particularly in the development of drugs that require specific stereochemical properties for efficacy. Safety data should be consulted for handling and usage, as with all chemical substances.

Formula: C₉H₁₃NO₂

InChI: InChI=1S/C9H13NO2/c10-8(6-11)9(12)7-4-2-1-3-5-7/h1-5,8-9,11-12H,6,10H2/t8-,9-/m1/s1

InChI key: InChIKey=JUCGVCVPNPBJIG-RKDXNWHRSA-N

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

Synonyms:

• (1R,2R)-(-)-2-Amino-1-phenyl-propane-1,3-diol
• (1R,2R)-1,3-dihydroxy-1-phenylpropan-2-aminium
• (1R,2R)-2-Amino-1-phenylpropan-1,3-diol
• (1R,2R)-2-Amino-1-phenylpropane-1,3-diol
• (1S,2R)-2-amino-1-phenylpropane-1,3-diol
• (R(R*,R*))-2-Amino-1-phenylpropane-1,3-diol
• 1,3-Propanediol, 2-amino-1-phenyl-, (1R,2R)-
• 1,3-Propanediol, 2-amino-1-phenyl-, [R-(R*,R*)]-
• <span class="text-smallcaps">D</span>-threo-1-Phenyl-2-amino-1,3-propanediol
• <span class="text-smallcaps">D</span>-threo-3-Phenyl-2-amino-1,3-propanediol
• (1R,2R)-2-Amino-1-phenyl-1,3-propanediol
• D-threo-3-Phenyl-2-amino-1,3-propanediol

(1R,2R)-2-amino-1-phenylpropane-1,3-diol

CAS: 46032-98-8

Formula: C₉H₁₃NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 167.2050

Ref: IN-DA003BGH

(1S,2S)-(-)-2-Amino-1-phenyl-1,3- propanediol

CAS: 46032-98-8

Ref: 7W-GK9571

(1R,2R)-(-)-2-Amino-1-phenyl-1,3-propanediol

CAS: 46032-98-8

(1R,2R)-(-)-2-Amino-1-phenyl-1,3-propanediol

Purity: 99%

Color and Shape: Solid

Molecular weight: 167.21g/mol

Ref: 54-OR322610

(1R,2R)-2-Amino-1-phenylpropane-1,3-diol

CAS: 46032-98-8

Purity: 97%

Color and Shape: Solid

Molecular weight: 167.2079926

Ref: 10-F791069

(1R,2R)-(-)-2-Amino-1-phenyl-1,3-propanediol

Controlled Product

CAS: 46032-98-8

Formula: C₉H₁₃NO₂

Color and Shape: Neat

Molecular weight: 167.2

Ref: TR-A636763

(1R,2R)-(-)-2-Amino-1-phenyl-1,3-propanediol

CAS: 46032-98-8

(1R,2R)-(-)-2-Amino-1-phenyl-1,3-propanediol is a chiral amino alcohol that can be used as a catalyst to catalyze the formation of aryl ketones. The reaction proceeds via an enantioselective addition of the amine to the carbonyl group in the presence of base. This reaction is also applicable to nucleosides, which are important in DNA replication and RNA transcription. Experiments have shown that (1R,2R)-(-)-2-Amino-1-phenyl-1,3-propanediol catalyzes bond formation between ribosome components and peptide bonds during protein synthesis.

Purity: Min. 95%

Ref: 3D-FA11703