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Molecule
ID:17976
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₀N₂O₂
Molecular Mass
178.1879
Exact Mass
178.07422757
Charge
0
InChI
InChI=1S/C9H10N2O2/c1-5-9(12)11-7-4-6(10)2-3-8(7)13-5/h2-5H,10H2,1H3,(H,11,12)
InChIKey
SUYYYBBFOLGROC-UHFFFAOYSA-N
Canonic Smiles
O=C1Nc2cc(N)ccc2OC1C
Isomeric Smiles
N1C(=O)C(Oc2c1cc(N)cc2)C
Calculated Properties
JChem
Acid pKa
11.491116
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
0.4477765
LogD (pH = 7.4)
0.49379843
Log P
0.49445224
Molar Refractivity
50.0194
Polarizability
18.155321
Polar Surface Area
64.35
Rotatable Bonds
0
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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Product Information
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
020039
Apollo Scientific
OR13750
Enamine
EN300-14821
A&J Pharmtech
AJA-O35345
Academic Data
PubChem
6483753
Names and Identifiers
IUPAC Traditional name
6-amino-2-methyl-2,4-dihydro-1,4-benzoxazin-3-one
IUPAC name
6-amino-2-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-one
Synonyms
6-Amino-2-methyl-2H-1,4-benzoxazin-3(4H)-one
6-Amino-2-methyl-4H-benzo[1,4]oxazin-3-one
Registration numbers
MDL Number
MFCD01834022
CAS Number
105807-80-5
PubChem CID
6483753
PubChem SID
160981283
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
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Source
Storage Warning
IRRITANT
Source
Irritant
Source
Physical Property
Melting Point
198 - 200°C
Source
0.224
Source
Product Information
95%
Source
98%
Source
Hydrophobicity(logP)
Purity