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Molecule
ID:24607
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₈N₂O
Molecular Mass
170.25202
Exact Mass
170.14191321
Charge
0
InChI
InChI=1S/C9H18N2O/c1-3-10-4-2-9(1)11-5-7-12-8-6-11/h9-10H,1-8H2
InChIKey
YYBXNWIRMJXEQJ-UHFFFAOYSA-N
Canonic Smiles
N1CCC(CC1)N1CCOCC1
Isomeric Smiles
N1(C2CCNCC2)CCOCC1
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-4.6435723
LogD (pH = 7.4)
-3.1279662
Log P
-0.3845728
Molar Refractivity
49.219
Polarizability
19.593437
Polar Surface Area
24.5
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
No Data Available
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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
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
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CAS Number
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PubChem SID
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MDL Number
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PubChem CID
Properties
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Safety Information
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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
ChemBridge
4004473
Matrix Scientific
027114
Apollo Scientific
OR0953
Sigma Aldrich
578045
Bide Pharmatech
BD34000
A&J Pharmtech
AJA-O2969
Academic Data
PubChem
795724
Names and Identifiers
Synonyms
4-Piperidin-4-ylmorpholine
4-(Piperidin-4-yl)morpholine 98+%
4-(Morpholin-4-yl)piperidine
4-Morpholinopiperidine
4-吗啉哌啶
4-(4-Piperidinyl) morpholine
4-Morpholinopiperidine
4-(Piperidin-4-yl)Morpholine
IUPAC Traditional name
4-(piperidin-4-yl)morpholine
IUPAC name
4-(piperidin-4-yl)morpholine
Registration numbers
CAS Number
53617-35-9
PubChem SID
24880906
160987914
MDL Number
MFCD03274733
PubChem CID
795724
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Harmful/Irritant/Air Sensitive/Store under Argon
Source
GHS Precautionary statements
P261
-
P305+P351+P338
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 Signal Word
Warning
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Risk Statements
36/37/38
Source
European Hazard Symbols
Irritant (Xi)
Source
Safety Statements
26
-
36
Source
Physical Property
Melting Point
40-43°C
Source
40-43 °C(lit.)
Source
Boiling Point
100-115°C/0.15mm
Source
100-115 °C/0.15-0.20 mmHg(lit.)
Source
Product Information
Empirical Formula (Hill Notation)
C9H16N2O
Source
Purity
98%
Source
95+%
Source
97%
Source
Molecule Details
Sigma Aldrich
578045
Packaging
1, 5 g in glass bottle
Application
Reactant for synthesis of:
• Selective adenosine A2A receptor antagonists1
• Antidepressents2
• Small molecules that restore E-cadherin expression and reduce invasion in colorectal carcinoma cells3
• Orally bioavailable P2Y12 antagonists for inhibition of platelet aggregation4
• Quinoline derivatives with antimicrobial activity5
• Antimalarials6
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay