CAS 76985-10-9

(αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-naphthalenepropanoic acid

Description:

The chemical substance known as (αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-naphthalenepropanoic acid, with the CAS number 76985-10-9, is an amino acid derivative characterized by its complex structure that includes a naphthalene moiety. This compound features a chiral center, which contributes to its stereochemical properties, specifically the (αR) configuration. The presence of the dimethylethoxycarbonyl group indicates that it has protective functionalities, commonly used in organic synthesis to enhance stability and solubility. The naphthalene ring system provides aromatic characteristics, which can influence the compound's reactivity and interaction with biological systems. This substance may exhibit specific biological activities, making it of interest in pharmaceutical research, particularly in the development of drugs targeting various biological pathways. Its solubility, stability, and reactivity can be influenced by the functional groups present, making it a versatile compound in synthetic organic chemistry and medicinal chemistry applications.

Formula: C₁₈H₂₁NO₄

InChI: InChI=1S/C18H21NO4/c1-18(2,3)23-17(22)19-15(16(20)21)11-12-8-9-13-6-4-5-7-14(13)10-12/h4-10,15H,11H2,1-3H3,(H,19,22)(H,20,21)/t15-/m1/s1

InChI key: InChIKey=URKWHOVNPHQQTM-OAHLLOKOSA-N

SMILES: C([C@@H](NC(OC(C)(C)C)=O)C(O)=O)C1=CC2=C(C=C1)C=CC=C2

Synonyms:

• (2R)-2-[(2-Methylpropan-2-yl)oxycarbonylamino]-3-naphthalen-2-ylpropanoic acid
• (R)-2-[(tert-Butoxycarbonyl)amino]-3-(naphthalen-2-yl)propionic acid
• (R)-N-BOC-2-Naphthylalanine
• (αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-naphthalenepropanoic acid
• 2-Naphthalenepropanoic acid α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αR)-
• 2-Naphthalenepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)-
• BOC-(2-naphthyl)-<span class="text-smallcaps">D</span>-alanine
• Boc-3-(2-Naphthyl)-D-alanine
• Boc-D-2-Nal-OH
• Boc-D-3-(2-Naphthyl)-alanine
• N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-<span class="text-smallcaps">D</span>-alanine
• N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-D-alanine

Boc-D-2-Nal-OH

CAS: 76985-10-9

Bachem ID: 4011831.

Formula: C₁₈H₂₁NO₄

Purity: > 99%

Color and Shape: Whitish

Molecular weight: 315.37

Ref: 01-4011831

N-tert-Butoxycarbonyl-2-naphthyl-D-alanine

CAS: 76985-10-9

Formula: C₁₈H₂₁NO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 315.3636

Ref: IN-DA0036HU

3-Naphth-2-yl-D-alanine, N-BOC protected

CAS: 76985-10-9

3-Naphth-2-yl-D-alanine, N-BOC protected

Formula: C₁₈H₂₁NO₄

Purity: ≥95%

Color and Shape: white solid

Molecular weight: 315.36363g/mol

Ref: 54-OR14599

Boc-D-2-Nal-OH

CAS: 76985-10-9

Formula: C₁₈H₂₁NO₄

Molecular weight: 315.37

Ref: 7W-GM2889

N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-D-alanine

CAS: 76985-10-9

Formula: C₁₈H₂₁NO₄

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 315.37

Ref: 3B-B3616

Boc-3-(2-Naphthyl)-D-alanine

CAS: 76985-10-9

M03151 - Boc-3-(2-Naphthyl)-D-alanine

Formula: C₁₈H₂₁NO₄

Purity: 98%

Color and Shape: Solid, White powder

Molecular weight: 315.369

Ref: 10-M03151

Boc-3-(2-Naphthyl)-D-alanine

Controlled Product

CAS: 76985-10-9

Applications Boc-3-(2-Naphthyl)-D-alanine is a reagent in Lanreotide trisulfide synthesis and somatostatin receptor binding activity. Reagent in the preparation by coupling and structure-activity relationships of arginine containing tripeptides as MC4 receptor ligands.
References Chen, L., et al.: Peptides: Frontiers of Peptide Science, Proceedings of the American Peptide Symposium, 275 (1999); Nozawa, D., et al.: Chem. Pharm. Bull., 55, 1232 (2007)

Formula: C₁₈H₂₁NO₄

Color and Shape: Neat

Molecular weight: 315.36

Ref: TR-B667360