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Molecule
ID:48615
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₃BrN₂
Molecular Mass
241.12762
Exact Mass
240.02621043
Charge
0
InChI
InChI=1S/C10H13BrN2/c1-8-6-9(11)7-12-10(8)13-4-2-3-5-13/h6-7H,2-5H2,1H3
InChIKey
BZEGKJPCIKOKKL-UHFFFAOYSA-N
Canonic Smiles
Brc1cnc(c(c1)C)N1CCCC1
Isomeric Smiles
c1(ncc(cc1C)Br)N1CCCC1
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
3.0007508
LogD (pH = 7.4)
3.1438506
Log P
3.1460462
Molar Refractivity
58.8482
Polarizability
21.74735
Polar Surface Area
16.13
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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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
Calculated Properties
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IUPAC Traditional name
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IUPAC name
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MDL Number
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
53410200
Commercial Catalog
Matrix Scientific
052103
Names and Identifiers
IUPAC Traditional name
5-bromo-3-methyl-2-(pyrrolidin-1-yl)pyridine
IUPAC name
5-bromo-3-methyl-2-(pyrrolidin-1-yl)pyridine
Synonyms
5-Bromo-3-methyl-2-(1-pyrrolidinyl)pyridine
Registration numbers
PubChem SID
162053378
PubChem CID
53410200
MDL Number
MFCD13561910
Properties
Safety Information
MSDS Link
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Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay