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Molecule
ID:38581
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₂₀N₂O₄
Molecular Mass
232.2768
Exact Mass
232.14230713
Charge
0
InChI
InChI=1S/C10H20N2O4/c1-10(2,3)16-9(15)11-7(8(13)14)6-12(4)5/h7H,6H2,1-5H3,(H,11,15)(H,13,14)/t7-/m0/s1
InChIKey
VCDQZVYJKDSORW-ZETCQYMHSA-N
Canonic Smiles
CN(C[C@@H](C(=O)O)NC(=O)OC(C)(C)C)C
Isomeric Smiles
CN(C[C@@H](C(=O)O)NC(=O)OC(C)(C)C)C
Calculated Properties
JChem
Acid pKa
3.1258228
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
-2.1517777
LogD (pH = 7.4)
-2.1831787
Log P
-2.1516914
Molar Refractivity
58.6408
Polarizability
23.16858
Polar Surface Area
78.87
Rotatable Bonds
6
Lipinski's Rule of Five
true
Data Source
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
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Academic Data
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Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
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MDL Number
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PubChem CID
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PubChem SID
Properties
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
17998956
Commercial Catalog
Matrix Scientific
041470
Names and Identifiers
IUPAC Traditional name
(2S)-2-[(tert-butoxycarbonyl)amino]-3-(dimethylamino)propanoic acid
IUPAC name
(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(dimethylamino)propanoic acid
Synonyms
Boc-aza-L-leucine
Registration numbers
MDL Number
MFCD02682423
PubChem CID
17998956
PubChem SID
161001888
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
TSCA Listed
false
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay