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Molecule
ID:67349
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₇N₃O₂
Molecular Mass
153.13868
Exact Mass
153.05382648
Charge
0
InChI
InChI=1S/C6H7N3O2/c1-4-2-3-5(9(10)11)6(7)8-4/h2-3H,1H3,(H2,7,8)
InChIKey
LCJXSRQGDONHRK-UHFFFAOYSA-N
Canonic Smiles
[O-][N+](=O)c1ccc(nc1N)C
Isomeric Smiles
c1(c(ccc(n1)C)[N+](=O)[O-])N
Calculated Properties
JChem
Acid pKa
16.256609
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
1.2410464
LogD (pH = 7.4)
1.2424415
Log P
1.2424593
Molar Refractivity
39.827
Polarizability
14.276094
Polar Surface Area
82.05
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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References
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Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
OR3342
Matrix Scientific
072772
076681
Enamine
EN300-98487
Bide Pharmatech
BD3628
A&J Pharmtech
AJA-O38705
Academic Data
PubChem
226028
Names and Identifiers
Synonyms
2-Amino-3-nitro-6-picoline
2-Amino-6-methyl-3-nitropyridine 95%
6-Methyl-3-nitro-pyridin-2-ylamine
6-methyl-3-nitropyridin-2-amine
2-AMINO-6-METHYL-3-NITROPYRIDINE
IUPAC Traditional name
6-methyl-3-nitropyridin-2-amine
IUPAC name
6-methyl-3-nitropyridin-2-amine
Registration numbers
CAS Number
21901-29-1
MDL Number
MFCD00047443
PubChem SID
162033084
PubChem CID
226028
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
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Storage Warning
IRRITANT
Source
Irritant
Source
Product Information
95+%
Source
95%
Source
98%
Source
Physical Property
1.364
Source
149 - 151°C
Source
Purity
Hydrophobicity(logP)
Melting Point