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Molecule
ID:102131
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₄N₂O
Molecular Mass
214.26306
Exact Mass
214.11061308
Charge
0
InChI
InChI=1S/C13H14N2O/c1-9(14)13(16)15-12-7-6-10-4-2-3-5-11(10)8-12/h2-9H,14H2,1H3,(H,15,16)/t9-/m0/s1
InChIKey
RQHPADKWNYTHOH-VIFPVBQESA-N
Canonic Smiles
O=C([C@@H](N)C)Nc1ccc2c(c1)cccc2
Isomeric Smiles
C[C@H](N)C(=O)Nc1cc2c(cccc2)cc1
Calculated Properties
JChem
Acid pKa
13.247552
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
-0.7086829
LogD (pH = 7.4)
0.96001
Log P
1.8450674
Molar Refractivity
65.2248
Polarizability
26.139515
Polar Surface Area
55.12
Rotatable Bonds
2
Lipinski's Rule of Five
true
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General Information
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IUPAC name
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MP Biomedicals
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Data Source
Commercial Catalog
MP Biomedicals
02100290
Sigma Aldrich
A2628
Academic Data
PubChem
688372
Names and Identifiers
IUPAC name
(2S)-2-amino-N-(naphthalen-2-yl)propanamide
IUPAC Traditional name
(2S)-2-amino-N-(naphthalen-2-yl)propanamide
Synonyms
L-ALANINE-β-NAPHTHYLAMIDE HYDROBROMIDE
L-Alanine β-naphthylamide
Registration numbers
CAS Number
3513-56-2
720-82-1
PubChem CID
688372
PubChem SID
162088381
24890677
EC Number
211-956-5
MDL Number
MFCD00064969
Properties
Product Information
Certificate of Analysis
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Source
Purity
98%
Source
Empirical Formula (Hill Notation)
C13H14N2O
Source
Safety Information
MSDS Link
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Source
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Source
Storage Condition
0°C, Desiccate
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Storage Temperature
2-8°C
Source
Molecule Details
MP Biomedicals
02100290
Hydrobromide
Purity: 98%
References
PubChem Literature
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Bioactivity
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