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Molecule
ID:104400
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₃NO₂
Molecular Mass
215.24782
Exact Mass
215.09462866
Charge
0
InChI
InChI=1S/C13H13NO2/c14-12(13(15)16)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7,12H,8,14H2,(H,15,16)
InChIKey
OFYAYGJCPXRNBL-UHFFFAOYSA-N
Canonic Smiles
OC(=O)C(Cc1cccc2c1cccc2)N
Isomeric Smiles
NC(Cc1c2ccccc2ccc1)C(=O)O
Calculated Properties
JChem
Acid pKa
2.6140146
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-0.19483837
LogD (pH = 7.4)
-0.19827187
Log P
-0.19462584
Molar Refractivity
61.5665
Polarizability
25.420156
Polar Surface Area
63.32
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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Bioactivity
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Data Source
Commercial Catalog
MP Biomedicals
02155791
Sigma Aldrich
N5637
A&J Pharmtech
AJA-O38842
Academic Data
PubChem
99505
Names and Identifiers
Synonyms
DL-3-(1-NAPHTHYL)ALANINE
3-(1-Naphthyl)-DL-alanine
2-AMINO-3-NAPHTHALEN-1-YL-PROPIONIC ACID
IUPAC Traditional name
alphanaphthylalanine
IUPAC name
2-amino-3-(naphthalen-1-yl)propanoic acid
Registration numbers
CAS Number
28095-56-9
PubChem SID
24897744
162091534
MDL Number
MFCD00067507
PubChem CID
99505
Molecule Details
Sigma Aldrich
N5637
Biochem/physiol Actions
3-(1-Naphthyl)-DL-alanine is an amino acid derivative that has been used to synthesize cholecystokinin analogues.
References
PubChem Literature
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Bioactivity
PubChem BioAssay
Properties
Product Information
Certificate of Analysis
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Purity
98%
Source
Safety Information
Storage Condition
2-8°C
Source
MSDS Link
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Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
2-8°C
Source
3
Source
Personal Protective Equipment
Storage Temperature
German water hazard class