Skip to Content
MilliporeSigma
All Photos(1)

Documents

578045

Sigma-Aldrich

4-Morpholinopiperidine

98%

Synonym(s):

4-(4-Piperidinyl) morpholine

Sign Into View Organizational & Contract Pricing


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

Assay

98%

bp

100-115 °C/0.15-0.20 mmHg (lit.)

mp

40-43 °C (lit.)

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

Application

4-Morpholinopiperidine may be used to synthesize 2-(4-morpholinopiperidin-1-yl)-5-nitrobenzonitrile 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.
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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

"A new phenylpyrazoleanilide, y-320, inhibits interleukin 17 production and ameliorates collagen-induced arthritis in mice and cynomolgus monkeys"
Ushio H, et al.
Pharmaceuticals (Basel, Switzerland), 7(01), 1-17 (2013)
"Design and synthesis of a highly selective, orally active and potent anaplastic lymphoma kinase inhibitor (CH5424802)"
Kinoshita K, et al.
Bioorganic & Medicinal Chemistry, 20(03), 1271-1280 (2012)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service