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Molecule
ID:64421
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₉NO₂
Molecular Mass
151.16256
Exact Mass
151.06332853
Charge
0
InChI
InChI=1S/C8H9NO2/c9-6-2-1-3-7-8(6)11-5-4-10-7/h1-3H,4-5,9H2
InChIKey
DMLRSJNZORFCBD-UHFFFAOYSA-N
Canonic Smiles
Nc1cccc2c1OCCO2
Isomeric Smiles
c12c(OCCO1)cccc2N
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
0.6457511
LogD (pH = 7.4)
0.6573031
Log P
0.6574524
Molar Refractivity
41.7158
Polarizability
15.783819
Polar Surface Area
44.48
Rotatable Bonds
0
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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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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RDKit
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JChem
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Academic Data
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IUPAC name
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IUPAC Traditional name
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CAS Number
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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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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR2819
Matrix Scientific
069747
Enamine
EN300-51150
Academic Data
PubChem
11788387
Names and Identifiers
Synonyms
2,3-Dihydro-1,4-benzodioxin-5-amine
2,3-Dihydro-1,4-benzodioxin-5-amine
5-Amino-2,3-dihydro-1,4-benzodioxine
IUPAC name
2,3-dihydro-1,4-benzodioxin-5-amine
IUPAC Traditional name
2,3-dihydro-1,4-benzodioxin-5-amine
Registration numbers
CAS Number
16081-45-1
MDL Number
MFCD03695459
PubChem SID
162030160
PubChem CID
11788387
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Toxic
Source
Product Information
Purity
98%
Source
95%
Source
Physical Property
56 - 58°C
Source
0.95
Source
Melting Point
Hydrophobicity(logP)