CAS 3082-64-2

(+)-1-Phenylpropylamine

Description:

(+)-1-Phenylpropylamine, with the CAS number 3082-64-2, is an organic compound characterized by its amine functional group and a phenyl group attached to a propyl chain. This chiral amine exists in two enantiomeric forms, with the (+) designation indicating its specific optical activity. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The compound is known for its potential applications in organic synthesis and as a building block in pharmaceuticals, particularly in the development of various biologically active molecules. Its basicity is attributed to the presence of the amine group, allowing it to participate in acid-base reactions. Additionally, (+)-1-Phenylpropylamine may exhibit varying solubility in polar and non-polar solvents, influencing its reactivity and utility in different chemical environments. Safety considerations should be taken into account when handling this compound, as with many amines, due to potential irritant properties and the need for proper storage conditions to maintain stability.

Formula: C₉H₁₃N

InChI: InChI=1S/C9H13N/c1-2-9(10)8-6-4-3-5-7-8/h3-7,9H,2,10H2,1H3/t9-/m1/s1

InChI key: InChIKey=AQFLVLHRZFLDDV-SECBINFHSA-N

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

Synonyms:

• (+)-((R)-1-Phenylpropyl)amine
• (+)-1-Ethylbenzylamine
• (+)-1-Phenylpropylamine
• (+)-α-Phenylpropylamine
• (1R)-1-Phenylpropylamine
• (1R)-1-phenylpropan-1-amine
• (1S)-1-phenylpropan-1-amine
• (R)-(+)-1-Amino-1-phenylpropane
• (R)-(+)-1-Phenyl-1-propylamine
• (R)-(+)-alpha-Ethylbenzylamine
• (R)-(+)-α-Phenyl-1-propylamine
• (R)-1-Phenyl-1-propanamine
• (R)-1-Phenylpropan-1-amine
• (R)-1-Phenylpropanamine
• (R)-α-Phenylpropylamine
• (αR)-α-Ethylbenzenemethanamine
• Benzenemethanamine, α-ethyl-, (R)-
• Benzenemethanamine, α-ethyl-, (αR)-
• Benzylamine, α-ethyl-, (R)-(+)-
• Benzylamine, α-ethyl-, d-

(R)-(+)-1-Phenylpropylamine, ChiPros 99+%, ee 98%

CAS: 3082-64-2

For synthesis of optically active products 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

Formula: C₉H₁₃N

Purity: 98%

Color and Shape: Clear colorless, Liquid

Molecular weight: 135.21

Ref: 02-L16319

(R)-(+)-1-Phenylpropylamine

CAS: 3082-64-2

Formula: C₉H₁₃N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 135.2062

Ref: IN-DA00327H

(R)-(+)-1-Phenylpropylamine

CAS: 3082-64-2

(R)-(+)-1-Phenylpropylamine

Purity: 95%

Molecular weight: 135.21g/mol

Ref: 54-OR912344

(R)-1-Phenylpropan-1-amine

CAS: 3082-64-2

Formula: C₉H₁₃N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 135.21

Ref: 10-F208825

(R)-(+)-α-Ethylbenzylamine

Controlled Product

CAS: 3082-64-2

Applications A chiral phenylalkylamine derivative used in metabolic Cytochrome P-455 nm complex formation studies.
References Joensson, K.H. et al.: Chirality, 4, 469 (1992);

Formula: C₉H₁₃N

Color and Shape: Neat

Molecular weight: 135.21

Ref: TR-E899970

(R)-(+)-1-Ethylbenzylamine

CAS: 3082-64-2

(R)-(+)-1-Ethylbenzylamine is a hydrogenated compound, which means that it contains at least one double bond. It also reacts with other molecules to form new compounds. It can be synthesized in an asymmetric synthesis, which means that the product can have different stereoisomers. This product has a primary amine group and a functional group on the same side of the molecule. The compound is expressed as a white crystalline solid and has been shown to react with glyoxylate to form an iminium ion. The iminium ion is five-membered and has two resonance structures, which are shown in the structural analysis.

Formula: C₉H₁₃N

Purity: Min. 95%

Molecular weight: 135.21 g/mol

Ref: 3D-FE165650