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Molecule
ID:102148
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₁IN₂O₅
Molecular Mass
354.09851
Exact Mass
353.97126946
Charge
0
InChI
InChI=1S/C9H11IN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)
InChIKey
XQFRJNBWHJMXHO-UHFFFAOYSA-N
Canonic Smiles
OCC1OC(CC1O)n1cc(I)c(=O)[nH]c1=O
Isomeric Smiles
OCC1OC(CC1O)n1cc(I)c(=O)[nH]c1=O
Calculated Properties
JChem
Acid pKa
8.056083
H Acceptors
5
H Donor
3
LogD (pH = 5.5)
-0.5301102
LogD (pH = 7.4)
-0.6144564
Log P
-0.5289186
Molar Refractivity
64.4039
Polarizability
25.542524
Polar Surface Area
99.1
Rotatable Bonds
2
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
Calculated Properties
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RDKit
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JChem
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Academic Data
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Synonyms
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IUPAC name
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IUPAC Traditional name
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EC Number
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CAS Number
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PubChem SID
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PubChem CID
Properties
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Product Information
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Physical Property
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Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02100357
Academic Data
PubChem
3687
Names and Identifiers
Synonyms
Idoxuridine
IDU
5-IODO-2'-DEOXYURIDINE
IUPAC name
1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-1,2,3,4-tetrahydropyrimidine-2,4-dione
IUPAC Traditional name
idoxuridine
Registration numbers
EC Number
200-207-8
CAS Number
54-42-2
PubChem SID
162089930
PubChem CID
3687
Properties
Product Information
Certificate of Analysis
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Source
Purity
~99%
Source
Physical Property
Melting Point
196-197°C
Source
Safety Information
RTECS
YU7700000
Source
MSDS Link
Download link
Source
Storage Condition
0°C, Protect from light
Source
Molecule Details
MP Biomedicals
02100357
Crystalline
Purity: ~99%
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay