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Molecule
ID:24866
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₅IN₂O₂
Molecular Mass
252.00987
Exact Mass
251.93957541
Charge
0
InChI
InChI=1S/C5H5IN2O2/c1-8-4(5(9)10)3(6)2-7-8/h2H,1H3,(H,9,10)
InChIKey
SZRMOKQNOJYMNK-UHFFFAOYSA-N
Canonic Smiles
Cn1ncc(c1C(=O)O)I
Isomeric Smiles
c1(n(ncc1I)C)C(=O)O
Calculated Properties
JChem
Acid pKa
3.186959
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.383429
LogD (pH = 7.4)
-2.5403523
Log P
0.9076344
Molar Refractivity
55.4576
Polarizability
16.836214
Polar Surface Area
55.12
Rotatable Bonds
1
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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Product Information
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
ChemBridge
4029192
Apollo Scientific
OR16973
Matrix Scientific
027388
Enamine
EN300-83506
Bide Pharmatech
BD172942
A&J Pharmtech
AJA-O9953
Academic Data
PubChem
673687
Names and Identifiers
Synonyms
4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acid
4-Iodo-2-methyl-2H-pyrazole-3-carboxylic acid
5-Carboxy-4-iodo-1-methyl-1H-pyrazole
4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acid 98%
IUPAC name
4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid
IUPAC Traditional name
4-iodo-2-methylpyrazole-3-carboxylic acid
Registration numbers
CAS Number
75092-30-7
MDL Number
MFCD00461121
PubChem SID
160988173
PubChem CID
673687
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Irritant/Light Sensitive/Keep Cold
Source
Physical Property
Melting Point
241-242°C
Source
0.689
Source
Product Information
95%
Source
95+%
Source
97%
Source
Hydrophobicity(logP)
Purity