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Molecule
ID:87292
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₄N₂O₅
Molecular Mass
242.22856
Exact Mass
242.09027156
Charge
0
InChI
InChI=1S/C10H14N2O5/c1-10(2,3)17-9(15)11-4-7-12-6(5-16-7)8(13)14/h5H,4H2,1-3H3,(H,11,15)(H,13,14)
InChIKey
AKUIDVVQFDMLAW-UHFFFAOYSA-N
Canonic Smiles
O=C(OC(C)(C)C)NCc1occ(n1)C(=O)O
Isomeric Smiles
o1c(nc(c1)C(=O)O)CNC(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
3.9244998
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
-0.9324879
LogD (pH = 7.4)
-2.5511606
Log P
0.6496027
Molar Refractivity
56.325
Polarizability
21.810871
Polar Surface Area
101.66
Rotatable Bonds
5
Lipinski's Rule of Five
true
Data Source
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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
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IUPAC Traditional name
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IUPAC name
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
OR30642
Academic Data
PubChem
11356912
Names and Identifiers
Synonyms
2-{[(tert-Butoxycarbonyl)amino]methyl}-1,3-oxazole-4-carboxylic acid
2-(Aminomethyl)-1,3-oxazole-4-carboxylic acid, 2-BOC protected
IUPAC Traditional name
2-{[(tert-butoxycarbonyl)amino]methyl}-1,3-oxazole-4-carboxylic acid
IUPAC name
2-({[(tert-butoxy)carbonyl]amino}methyl)-1,3-oxazole-4-carboxylic acid
Registration numbers
CAS Number
182120-90-7
PubChem CID
11356912
PubChem SID
162074403
Properties
Safety Information
Storage Warning
Irritant
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay