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Molecule
ID:13635
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₈N₂O₂
Molecular Mass
140.13992
Exact Mass
140.05857751
Charge
0
InChI
InChI=1S/C6H8N2O2/c1-5-7-2-3-8(5)4-6(9)10/h2-3H,4H2,1H3,(H,9,10)
InChIKey
DKLNXONACKSAQI-UHFFFAOYSA-N
Canonic Smiles
Cc1nccn1CC(=O)O
Isomeric Smiles
c1nc(n(c1)CC(=O)O)C
Calculated Properties
JChem
Acid pKa
3.7227356
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.6227088
LogD (pH = 7.4)
-1.9388857
Log P
-1.6384641
Molar Refractivity
34.4348
Polarizability
13.174284
Polar Surface Area
55.12
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Properties
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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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PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4009535
4087837
Matrix Scientific
011067
Life Chemicals
F2130-0093
InterBioScreen
BB_SC-5929
Enamine
EN300-41506
Academic Data
PubChem
650088
Names and Identifiers
IUPAC name
2-(2-methyl-1H-imidazol-1-yl)acetic acid
Synonyms
(2-methyl-1H-imidazol-1-yl)acetic acid
(2-Methyl-imidazol-1-yl)-acetic acid
(2-methyl-1H-imidazol-1-yl)acetic acid hydrochloride
2-(2-methyl-1H-imidazol-1-yl)acetic acid
IUPAC Traditional name
(2-methylimidazol-1-yl)acetic acid
Registration numbers
CAS Number
25023-36-3
MDL Number
MFCD03250177
MFCD06801036
PubChem SID
160976942
PubChem CID
650088
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Physical Property
Partition Coefficient
-0.131
Source
Hydrophobicity(logP)
-0.362
Source
Product Information
95+%
Source
95%
Source
HCl
Source
Purity
Salt Data