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Molecule
ID:43642
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₃N₃O₄
Molecular Mass
251.23862
Exact Mass
251.09060591
Charge
0
InChI
InChI=1S/C11H13N3O4/c1-18-11(15)9-3-2-6-13(9)10-5-4-8(7-12-10)14(16)17/h4-5,7,9H,2-3,6H2,1H3/t9-/m0/s1
InChIKey
NDZYRKDQBWLBHP-VIFPVBQESA-N
Canonic Smiles
COC(=O)[C@@H]1CCCN1c1ccc(cn1)[N+](=O)[O-]
Isomeric Smiles
c1(cnc(cc1)N1[C@@H](CCC1)C(=O)OC)[N+](=O)[O-]
Calculated Properties
JChem
H Acceptors
5
H Donor
0
LogD (pH = 5.5)
1.6396898
LogD (pH = 7.4)
1.63969
Log P
1.63969
Molar Refractivity
64.1079
Polarizability
23.632078
Polar Surface Area
88.25
Rotatable Bonds
4
Lipinski's Rule of Five
true
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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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MDL Number
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Product Information
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
046990
Key Organics
FA-0006
Academic Data
PubChem
18526130
Names and Identifiers
IUPAC Traditional name
methyl (2S)-1-(5-nitropyridin-2-yl)pyrrolidine-2-carboxylate
IUPAC name
methyl (2S)-1-(5-nitropyridin-2-yl)pyrrolidine-2-carboxylate
Synonyms
Methyl (2S)-1-(5-nitro-2-pyridinyl)tetrahydro-1H-pyrrole-2-carboxylate
Registration numbers
MDL Number
MFCD08689691
PubChem SID
162048405
PubChem CID
18526130
CAS Number
122092-22-2
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
87-88°C
Source
87 - 88 °C
Source
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
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Source
Product Information
>95%
Source
Purity