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About This Item
Empirical Formula (Hill Notation):
C9H18N2O
CAS Number:
Molecular Weight:
170.25
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
bp
100-115 °C/0.15-0.20 mmHg (lit.)
mp
40-43 °C (lit.)
functional group
ether
SMILES string
C1CC(CCN1)N2CCOCC2
InChI
1S/C9H18N2O/c1-3-10-4-2-9(1)11-5-7-12-8-6-11/h9-10H,1-8H2
InChI key
YYBXNWIRMJXEQJ-UHFFFAOYSA-N
1 of 4
This Item | 678813 | 591777 | H52201 |
|---|---|---|---|
| assay 98% | assay 97% | assay 97% | assay 99% |
| Quality Level 100 | Quality Level 200 | Quality Level 100 | Quality Level 100 |
| bp 100-115 °C/0.15-0.20 mmHg (lit.) | bp - | bp - | bp - |
| mp 40-43 °C (lit.) | mp 65-69 °C | mp 114-118 °C (lit.) | mp 157-161 °C (lit.) |
| functional group ether | functional group aldehyde, ether | functional group bromo, ether | functional group - |
Application
4-Morpholinopiperidine may be used to synthesize 2-(4-morpholinopiperidin-1-yl)-5-nitrobenzonitrile[1] and 9-bromo-6,6-dimethyl-8-(4-morpholin-4-yl-piperidin-1-yl)-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile.[2]
Reactant for synthesis of:
- Selective adenosine A2A receptor antagonists
- Antidepressents
- Small molecules that restore E-cadherin expression and reduce invasion in colorectal carcinoma cells
- Orally bioavailable P2Y12 antagonists for inhibition of platelet aggregation
- Quinoline derivatives with antimicrobial activity
- Antimalarials
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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