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Molecule
ID:40150
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₅BrN₂O₂
Molecular Mass
217.0201
Exact Mass
215.95343941
Charge
0
InChI
InChI=1S/C6H5BrN2O2/c7-3-1-4(6(10)11)5(8)9-2-3/h1-2H,(H2,8,9)(H,10,11)
InChIKey
IEPDTLRHISNBLB-UHFFFAOYSA-N
Canonic Smiles
Brc1cnc(c(c1)C(=O)O)N
Isomeric Smiles
c1(c(ncc(c1)Br)N)C(=O)O
Calculated Properties
JChem
Acid pKa
2.503638
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
0.27540872
LogD (pH = 7.4)
-1.3328468
Log P
0.7236216
Molar Refractivity
43.794
Polarizability
16.006487
Polar Surface Area
76.21
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
OR1871
Key Organics
11W-0705
Matrix Scientific
043121
Enamine
EN300-113866
Bide Pharmatech
BD9884
A&J Pharmtech
AJA-O35358
Academic Data
PubChem
737445
Names and Identifiers
IUPAC name
2-amino-5-bromopyridine-3-carboxylic acid
Synonyms
2-Amino-5-bromonicotinic acid
2-Amino-5-bromopyridine-3-carboxylic acid
2-Amino-5-bromonicotinic acid 95%
2-amino-5-bromopyridine-3-carboxylic acid
IUPAC Traditional name
2-amino-5-bromopyridine-3-carboxylic acid
Registration numbers
CAS Number
52833-94-0
MDL Number
MFCD01860227
PubChem CID
737445
PubChem SID
162044913
Properties
Product Information
Purity
95+%
Source
>95%
Source
95%
Source
98%
Source
Safety Information
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Irritant/Keep Cold
Source
TSCA Listed
false
Source
Physical Property
Melting Point
217-220°C
Source
253 - 255 °C
Source
Hydrophobicity(logP)
1.657
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay