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Molecule
ID:39210
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₁₉ClN₂O₄
Molecular Mass
338.78606
Exact Mass
338.10333478
Charge
0
InChI
InChI=1S/C16H19ClN2O4/c1-16(2,3)23-15(22)19-13(14(20)21)6-9-8-18-12-5-4-10(17)7-11(9)12/h4-5,7-8,13,18H,6H2,1-3H3,(H,19,22)(H,20,21)
InChIKey
PZZXAZAYKCNQAL-UHFFFAOYSA-N
Canonic Smiles
OC(=O)C(Cc1c[nH]c2c1cc(Cl)cc2)NC(=O)OC(C)(C)C
Isomeric Smiles
c1(ccc2c(c1)c(c[nH]2)CC(C(=O)O)NC(=O)OC(C)(C)C)Cl
Calculated Properties
JChem
Acid pKa
3.9742153
H Acceptors
3
H Donor
3
LogD (pH = 5.5)
1.7382666
LogD (pH = 7.4)
0.09884656
Log P
3.272519
Molar Refractivity
85.8806
Polarizability
34.566727
Polar Surface Area
91.42
Rotatable Bonds
6
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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General Information
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IUPAC Traditional name
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IUPAC name
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From Data Sources
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Data Source
Academic Data
PubChem
22309411
Commercial Catalog
Matrix Scientific
042116
Names and Identifiers
IUPAC Traditional name
2-[(tert-butoxycarbonyl)amino]-3-(5-chloro-1H-indol-3-yl)propanoic acid
IUPAC name
2-{[(tert-butoxy)carbonyl]amino}-3-(5-chloro-1H-indol-3-yl)propanoic acid
Synonyms
Boc-5-chloro-DL-tryptophan
Registration numbers
MDL Number
MFCD09264328
PubChem SID
161002517
PubChem CID
22309411
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
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References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay