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Molecule
ID:67363
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₈BrNO₂
Molecular Mass
230.05862
Exact Mass
228.9738405
Charge
0
InChI
InChI=1S/C8H8BrNO2/c1-2-12-8(11)6-3-4-7(9)10-5-6/h3-5H,2H2,1H3
InChIKey
NTOOSJSHTQNLKP-UHFFFAOYSA-N
Canonic Smiles
CCOC(=O)c1ccc(nc1)Br
Isomeric Smiles
C(=O)(c1ccc(nc1)Br)OCC
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
2.0901325
LogD (pH = 7.4)
2.090133
Log P
2.090133
Molar Refractivity
49.14
Polarizability
18.677156
Polar Surface Area
39.19
Rotatable Bonds
3
Lipinski's Rule of Five
true
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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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IUPAC name
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IUPAC Traditional name
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Synonyms
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MDL Number
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PubChem SID
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PubChem CID
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Product Information
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Molecular Spectra
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TRC
References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
072786
TRC
B686010
Chemik
CHH00319
Bide Pharmatech
BD159692
A&J Pharmtech
AJA-O6257
Academic Data
PubChem
14784668
Names and Identifiers
IUPAC name
ethyl 6-bromopyridine-3-carboxylate
IUPAC Traditional name
ethyl 6-bromopyridine-3-carboxylate
Synonyms
6-Bromonicotinic acid ethyl ester
Ethyl 6-bromonicotinate
Ethyl 2-Bromo-5-pyridinecarboxylate
6-Bromo-3-pyridinecarboxylic Acid Ethyl Ester
6-Bromo Nicotinic Acid Ethyl Ester
Registration numbers
CAS Number
132334-98-6
MDL Number
MFCD11111853
PubChem SID
162033098
PubChem CID
14784668
Molecule Details
TRC
B686010
A potential hypolipidemic agent; a nicotinic acid analog. Heterocyclic compounds affecting free fatty acid mobilization in vivo.
References
PubChem Literature
From Data Sources
•
Carlson, L.A., et al.: Acta Pharma. Suecica, 9, 289 (1972)
Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
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Storage Warning
IRRITANT
Source
Product Information
Purity
95+%
来源
97%
Source
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Source
Certificate of Analysis