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Molecule
ID:124308
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₀ClN₃
Molecular Mass
183.6381
Exact Mass
183.05632502
Charge
0
InChI
InChI=1S/C8H9N3.ClH/c1-5-10-7-3-2-6(9)4-8(7)11-5;/h2-4H,9H2,1H3,(H,10,11);1H
InChIKey
KAQBQAWEULIHIR-UHFFFAOYSA-N
Canonic Smiles
Nc1ccc2c(c1)[nH]c(n2)C.Cl
Isomeric Smiles
n1c([nH]c2c1ccc(c2)N)C.Cl
Calculated Properties
JChem
Acid pKa
13.6492605
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
-0.8272304
LogD (pH = 7.4)
0.029085806
Log P
0.55364275
Molar Refractivity
44.1096
Polarizability
17.565441
Polar Surface Area
54.7
Rotatable Bonds
0
Lipinski's Rule of Five
true
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Molecule Details
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Bioactivity
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Data Source
Commercial Catalog
InterBioScreen
BB_SC-8752
Enamine
EN300-24356
Bide Pharmatech
BD159729
Academic Data
PubChem
16383570
Names and Identifiers
Synonyms
2-methyl-1H-benzo[d]imidazol-6-amine hydrochloride
2-Methyl-1H-benzo[d]imidazol-5-amine hydrochloride
2-methyl-1H-benzimidazol-5-amine hydrochloride
IUPAC name
2-methyl-1H-1,3-benzodiazol-6-amine hydrochloride
2-methyl-1H-1,3-benzodiazol-5-amine hydrochloride
IUPAC Traditional name
2-methyl-3H-1,3-benzodiazol-5-amine hydrochloride
2-methyl-1H-1,3-benzodiazol-5-amine hydrochloride
Registration numbers
PubChem SID
162218661
PubChem CID
16383570
CAS Number
1571-93-3
MDL Number
MFCD08692030
Properties
Product Information
Salt Data
HCl
Source
Purity
95%
Source
95+%
Source
Physical Property
Hydrophobicity(logP)
1.282
Source
References
PubChem Literature
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Bioactivity
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