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Molecule
ID:82222
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₇NO
Molecular Mass
143.22668
Exact Mass
143.13101417
Charge
0
InChI
InChI=1S/C8H17NO/c10-8-4-7-9-5-2-1-3-6-9/h10H,1-8H2
InChIKey
PLRXAFVBCHEMGD-UHFFFAOYSA-N
Canonic Smiles
OCCCN1CCCCC1
Isomeric Smiles
N1(CCCO)CCCCC1
Calculated Properties
JChem
Acid pKa
15.933373
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-3.0033906
LogD (pH = 7.4)
-1.8201616
Log P
0.41039333
Molar Refractivity
43.2878
Polarizability
16.88203
Polar Surface Area
23.47
Rotatable Bonds
3
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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General Information
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IUPAC Traditional name
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IUPAC name
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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
Academic Data
PubChem
66032
Commercial Catalog
Sigma Aldrich
152935
Enamine
EN300-55444
Apollo Scientific
OR24928
Names and Identifiers
IUPAC Traditional name
piperidine-1-propanol
IUPAC name
3-(piperidin-1-yl)propan-1-ol
Synonyms
3-piperidinopropan-1-ol
1-(3-Hydroxypropyl)piperidine
1-哌啶丙醇
1-Piperidinepropanol
3-(piperidin-1-yl)propan-1-ol
Registration numbers
MDL Number
MFCD00023781
PubChem CID
66032
PubChem SID
162069341
24849267
CAS Number
104-58-5
EC Number
203-216-5
Molecule Details
Sigma Aldrich
152935
Packaging
5 g in glass bottle
Application
Reactant in: Mitsunobu reaction of intramolecular nitrile oxide-alkene cycloadditions1 Suzuki-coupling2Reactant for synthesis of: Histamine H3 receptor antagonists3 Protein lysine methyltransferase G9a inhibitors4 Serotonin-4 receptors antagonists5 Checkpoint kinase Chk2 inhibitors6
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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MDL Number
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PubChem CID
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PubChem SID
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CAS Number
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EC Number
Properties
Product Information
Empirical Formula (Hill Notation)
C8H17NO
Source
Purity
97%
Source
95%
Source
Physical Property
Flash Point
206.6 °F
Source
97 °C
Source
Boiling Point
94-95 °C/0.5 mmHg(lit.)
Source
Refractive Index
n20/D 1.4775(lit.)
Source
Density
0.944 g/mL at 25 °C(lit.)
Source
Hydrophobicity(logP)
1.028
Source
Safety Information
GHS Precautionary statements
P261
-
P305+P351+P338
Source
RTECS
TN2414500
Source
German water hazard class
3
Source
Safety Statements
26
-
36
Source
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
Warning
Source
Irritant (Xi)
dust mask type N95 (US), Eyeshields, Gloves
Source
H315
-
H319
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H335
Source
Download link
Source
36/37/38
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GHS Pictograms
GHS Signal Word
European Hazard Symbols
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Risk Statements