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Molecule
ID:78310
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₄H₁₈INO₄
Molecular Mass
391.20149
Exact Mass
391.02805606
Charge
0
InChI
InChI=1S/C14H18INO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-6-4-5-7-10(9)15/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m1/s1
InChIKey
CAPUJMUOMAUNOD-LLVKDONJSA-N
Canonic Smiles
O=C(OC(C)(C)C)N[C@@H](C(=O)O)Cc1ccccc1I
Isomeric Smiles
N([C@H](Cc1ccccc1I)C(=O)O)C(=O)OC(C)(C)C
Calculated Properties
JChem
Acid pKa
3.1723607
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.1954441
LogD (pH = 7.4)
0.048477326
Log P
3.498657
Molar Refractivity
83.3518
Polarizability
32.733547
Polar Surface Area
75.63
Rotatable Bonds
6
Lipinski's Rule of Five
true
Data Source
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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
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IUPAC name
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IUPAC Traditional name
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PubChem CID
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PubChem SID
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
OR18041
Academic Data
PubChem
51341944
Names and Identifiers
Synonyms
(2S)-2-[(tert-Butoxycarbonyl)amino]-3-(2-iodophenyl)propanoic acid
2-Iodo-L-phenylalanine, N-BOC protected
IUPAC name
(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(2-iodophenyl)propanoic acid
IUPAC Traditional name
(2R)-2-[(tert-butoxycarbonyl)amino]-3-(2-iodophenyl)propanoic acid
Registration numbers
CAS Number
273221-78-6
PubChem CID
51341944
PubChem SID
162043079
Properties
Safety Information
Storage Warning
Irritant/Keep Cold
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay