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Molecule
ID:32158
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₀N₂O
Molecular Mass
150.1778
Exact Mass
150.07931295
Charge
0
InChI
InChI=1S/C8H10N2O/c1-6-2-4-7(5-3-6)8(9)10-11/h2-5,11H,1H3,(H2,9,10)
InChIKey
NKJXMLIWSJATEE-UHFFFAOYSA-N
Canonic Smiles
O/N=C(/c1ccc(cc1)C)\N
Isomeric Smiles
C(=N\O)(/c1ccc(cc1)C)\N
Calculated Properties
JChem
Acid pKa
10.302096
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.1723102
LogD (pH = 7.4)
1.3993541
Log P
1.4039539
Molar Refractivity
44.1214
Polarizability
16.47106
Polar Surface Area
58.61
Rotatable Bonds
1
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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IUPAC Traditional name
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IUPAC name
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PubChem CID
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PubChem SID
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MDL Number
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Product Information
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
034855
Apollo Scientific
OR5904
Life Chemicals
F2158-1171
Sigma Aldrich
548707
Academic Data
PubChem
5493168
Names and Identifiers
IUPAC Traditional name
(Z)-N'-hydroxy-4-methylbenzene-1-carboximidamide
N'-hydroxy-4-methylbenzenecarboximidamide
IUPAC name
(Z)-N'-hydroxy-4-methylbenzene-1-carboximidamide
N'-hydroxy-4-methylbenzene-1-carboximidamide
Synonyms
4-Methylbenzamide oxime
N'-Hydroxy-4-methylbenzamidine
N'-Hydroxy-4-methylbenzenecarboximidamide
4-Methylbenzamidoxime
4-甲基苯甲酰胺肟
4-Methylbenzamide oxime
p-Toluamideoxime
对甲苯酰胺肟
N'-hydroxy-4-methylbenzenecarboximidamide
Registration numbers
PubChem CID
5493168
PubChem SID
160995465
24879052
CAS Number
19227-13-5
MDL Number
MFCD00019952
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
Risk Statements
36/37/38
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
European Hazard Symbols
Irritant (Xi)
Source
RTECS
XS4870000
Source
German water hazard class
3
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
GHS Signal Word
Warning
Source
Safety Statements
26
-
36
Source
Physical Property
Melting Point
142-146°C
Source
140-145 °C(lit.)
Source
Partition Coefficient
1.763
Source
Product Information
Purity
97%
Source
95+%
Source
Linear Formula
CH3C6H4C(NH2)=NOH
Source
Molecule Details
Sigma Aldrich
548707
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay