CAS 3326-63-4

(αS)-α-Amino-N-2-naphthalenyl-1H-indole-3-propanamide

Description:

(αS)-α-Amino-N-2-naphthalenyl-1H-indole-3-propanamide, with the CAS number 3326-63-4, is a chemical compound that belongs to the class of amino acids and derivatives. It features a naphthalene moiety, which contributes to its aromatic characteristics, and an indole structure, known for its presence in various biologically active compounds. This compound exhibits chiral properties due to the presence of an α-amino group, which can influence its biological activity and interactions. It is typically characterized by its ability to participate in hydrogen bonding and π-π stacking interactions due to its aromatic components. The compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, owing to its structural features that can interact with biological targets. Its solubility, stability, and reactivity can vary depending on the specific conditions, such as pH and solvent, making it important to consider these factors in practical applications.

Formula: C₂₁H₁₉N₃O

InChI: InChI=1/C21H19N3O/c22-19(12-16-13-23-20-8-4-3-7-18(16)20)21(25)24-17-10-9-14-5-1-2-6-15(14)11-17/h1-11,13,19,23H,12,22H2,(H,24,25)/t19-/m0/s1

InChI key: InChIKey=FVGGFBMEWGARAX-IBGZPJMESA-N

SMILES: C([C@@H](C(NC1=CC2=C(C=C1)C=CC=C2)=O)N)C=3C=4C(NC3)=CC=CC4

Synonyms:

• (2S)-2-Amino-3-(1H-indol-3-yl)-N-naphthalen-2-ylpropanamide
• (S)-2-Amino-3-(1H-indol-3-yl)-N-naphthalen-2-ylpropionamide
• (αS)-α-Amino-N-2-naphthalenyl-1H-indole-3-propanamide
• 1H-Indole-3-propanamide, α-amino-N-2-naphthalenyl-, (S)-
• 1H-Indole-3-propanamide, α-amino-N-2-naphthalenyl-, (αS)-
• <span class="text-smallcaps">L</span>-Tryptophan-β-naphthylamide
• <span class="text-smallcaps">L</span>-Tryptophanyl β-naphthylamide
• H-Trp-.beta.NA
• H-Trp-Betana
• Indole-3-propionamide, α-amino-N-2-naphthyl-, <span class="text-smallcaps">L</span>-
• L-Tryptophan-?-naphthylamide
• N-naphthalen-2-yl-L-tryptophanamide
• N-naphthalen-2-yltryptophanamide
• Tryptophan-β-naphthylamide
• L-Tryptophanyl β-naphthylamide
• Indole-3-propionamide, α-amino-N-2-naphthyl-, L-
• N-(2-Naphtyl)-L-tryptophanamide
• L-tryptophan 2-naphthylamide
• L-Tryptophan β-naphthylamide
• H-Trp-bNA
• L-Tryptophan β-naphthylamide≥ 99% (TLC)
• H-Trp-βNA
• (S)-alpha-amino-N-2-naphthyl-1H-indole-3-propionamide
• (3R)-2,3-dihydro-1,4-benzodioxine-3-carboxamide
• L-TRYPTOPHAN-á-NAPHTHYLAMIDE
• L-Trp-βNA
• L-TRYPTOPHAN-BETA-NAPHTHYLAMIDE
• (S)-α-Amino-N-(2-naphthalenyl)-1H-indole-3-propanamide
• 2-azanyl-3-(1H-indol-3-yl)-N-naphthalen-2-yl-propanamide
• TRYPTOPHAN-BETANA
• L-tryptophan B-naphthylamide
• 2-amino-3-(1H-indol-3-yl)-N-naphthalen-2-ylpropanamide

L-Tryptophan-β-naphthylamide

CAS: 3326-63-4

Formula: C₂₁H₁₉N₃O

Purity: 95%

Molecular weight: 329.3951

Ref: IN-DA00I6HR

L-Tryptophan β-naphthylamide

CAS: 3326-63-4

Molecular weight: 329.40

Ref: 7W-GM8364

L-Tryptophan β-naphthylamide

CAS: 3326-63-4

L-Tryptophan beta-naphthylamide is a fine chemical that is useful for research purposes. It can be used as a versatile building block in the synthesis of other chemicals and can also be used as a reaction component. L-Tryptophan beta-naphthylamide has been used to synthesize complex compounds such as 5,6-dihydroindolizine, which has been shown to have anti-inflammatory properties. This compound can also be used as a reagent in organic synthesis.

Formula: C₂₁H₁₉N₃O

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 329.4 g/mol

Ref: 3D-FT48218

H-Trp-βNA

CAS: 3326-63-4

Bachem ID: 4002361.

Formula: C₂₁H₁₉N₃O

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 329.4

Ref: 01-4002361