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Molecule
ID:24783
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₈N₂O
Molecular Mass
206.28412
Exact Mass
206.14191321
Charge
0
InChI
InChI=1S/C12H18N2O/c1-15-12-4-2-11(3-5-12)10-14-8-6-13-7-9-14/h2-5,13H,6-10H2,1H3
InChIKey
MGLUVVBFISROAH-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cc1)CN1CCNCC1
Isomeric Smiles
N1(Cc2ccc(cc2)OC)CCNCC1
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-1.9574746
LogD (pH = 7.4)
-0.6244322
Log P
1.221043
Molar Refractivity
61.8193
Polarizability
24.388472
Polar Surface Area
24.5
Rotatable Bonds
3
Lipinski's Rule of Five
true
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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
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RDKit
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IUPAC name
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Synonyms
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IUPAC Traditional name
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PubChem SID
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PubChem CID
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CAS Number
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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
ChemBridge
3002373
Matrix Scientific
027299
Sigma Aldrich
646156
Academic Data
PubChem
231905
Names and Identifiers
IUPAC name
1-[(4-methoxyphenyl)methyl]piperazine
Synonyms
1-(4-Methoxybenzyl)piperazine
1-(4-甲氧基苄基)哌嗪
1-(4-Methoxybenzyl)piperazine
IUPAC Traditional name
1-[(4-methoxyphenyl)methyl]piperazine
Registration numbers
PubChem SID
160988090
24883436
PubChem CID
231905
CAS Number
21867-69-6
MDL Number
MFCD01075236
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
European Hazard Symbols
Harmful (Xn)
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H302
-
H319
Source
GHS Precautionary statements
P305+P351+P338
Source
Risk Statements
22
Source
German water hazard class
2
Source
Physical Property
Melting Point
32-36 °C(lit.)
Source
Flash Point
>230 °F
Source
>110 °C
Source
Product Information
Purity
97%
Source
Empirical Formula (Hill Notation)
C12H18N2O
Source
Molecule Details
Sigma Aldrich
646156
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay