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Molecule
ID:12206
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₉NO
Molecular Mass
123.15246
Exact Mass
123.06841391
Charge
0
InChI
InChI=1S/C7H9NO/c8-5-6-3-1-2-4-7(6)9/h1-4,9H,5,8H2
InChIKey
KPRZOPQOBJRYSW-UHFFFAOYSA-N
Canonic Smiles
NCc1ccccc1O
Isomeric Smiles
c1(c(cccc1)CN)O
Calculated Properties
JChem
Acid pKa
8.32269
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
-2.154139
LogD (pH = 7.4)
-1.0316718
Log P
-0.18066746
Molar Refractivity
36.5123
Polarizability
14.301682
Polar Surface Area
46.25
Rotatable Bonds
1
Lipinski's Rule of Five
true
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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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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
009264
Apollo Scientific
OR12317
TRC
H809725
Enamine
EN300-64465
Bide Pharmatech
BD62833
Academic Data
PubChem
70267
Names and Identifiers
Synonyms
2-(Aminomethyl)phenol
2-Hydroxybenzylamine
(2-Hydroxyphenyl)methylamine
Salicylamine
α-Amino-o-cresol
2-Hydroxybenzylamine
2-(Aminomethyl)phenol
NSC 127870
o-Hydroxybenzylamine
2-Hydroxybenzenemethanamine
IUPAC name
2-(aminomethyl)phenol
IUPAC Traditional name
2-(aminomethyl)phenol
Registration numbers
MDL Number
MFCD00870498
CAS Number
932-30-9
PubChem CID
70267
PubChem SID
160975513
Molecule Details
TRC
H809725
A potent γ-ketoaldehyde scavenger that has been shown to protects cardiac sodium channel (NaV1.5) from oxidant-induced inactivation
References
PubChem Literature
From Data Sources
•
Davies, S.S. et al.: Biochem., 45, 15756 (2010)
•
Zagol-Ikapitte, I. et al.: Pharmaceutics, 2, 18 (2010)
•
Nakajima, T. et al.: J. Mol. Cell. Cardiol., 48, 352 (2010)
Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
126-129°C
Source
125-126°C
Source
126 - 128°C
Source
Hydrophobicity(logP)
0.377
Source
Safety Information
MSDS Link
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Source
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Source
false
Source
Irritant/Store under Argon
Source
Product Information
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Source
95%
Source
95+%
Source
TSCA Listed
Storage Warning
Certificate of Analysis
Purity