1-morpholin-2-ylethanone

C6H11NO2 — CID 22263552

IUPAC1-morpholin-2-ylethanone
SMILESCC(=O)C1CNCCO1
InChIInChI=1S/C6H11NO2/c1-5(8)6-4-7-2-3-9-6/h6-7H,2-4H2,1H3
InChIKeySUKQFFFOGFYYHR-UHFFFAOYSA-N
MW129.16 g/mol
LogP-0.44
Rot. Bonds1

About 1-morpholin-2-ylethanone

1-morpholin-2-ylethanone (PubChem CID 22263552) has the molecular formula C6H11NO2 and a molecular weight of 129.16 g/mol. Its IUPAC name is 1-morpholin-2-ylethanone.

Molecular Properties

Compound Name1-morpholin-2-ylethanone
PubChem CID22263552
Molecular FormulaC6H11NO2
Molecular Weight129.16 g/mol
Exact Mass129.08
IUPAC Name1-morpholin-2-ylethanone
SMILESCC(=O)C1CNCCO1
InChIInChI=1S/C6H11NO2/c1-5(8)6-4-7-2-3-9-6/h6-7H,2-4H2,1H3
InChIKeySUKQFFFOGFYYHR-UHFFFAOYSA-N
XLogP-0.44
TPSA38.33 Ų
H-Bond Donors1
H-Bond Acceptors3
Rotatable Bonds1
Heavy Atoms9
Complexity—

Lipinski Rule of Five

Passes Rule of Five

RuleValue
MW ≤ 500129.16
LogP ≤ 5-0.44
H-Bond Donors ≤ 51
H-Bond Acceptors ≤ 103

Analyze 1-morpholin-2-ylethanone with MolForge

Explore ADMET properties, 3D molecular structure, drug-likeness score, and discover similar compounds using our AI-powered platform.

Launch Full Analysis

Frequently Asked Questions

What is the IUPAC name of 1-morpholin-2-ylethanone?
The IUPAC name of 1-morpholin-2-ylethanone (CID 22263552) is 1-morpholin-2-ylethanone.
What is the SMILES notation for 1-morpholin-2-ylethanone?
The canonical SMILES for 1-morpholin-2-ylethanone is CC(=O)C1CNCCO1.
What is the InChIKey of 1-morpholin-2-ylethanone?
The InChIKey is SUKQFFFOGFYYHR-UHFFFAOYSA-N. The full InChI is InChI=1S/C6H11NO2/c1-5(8)6-4-7-2-3-9-6/h6-7H,2-4H2,1H3.
What are the key properties of 1-morpholin-2-ylethanone?
1-morpholin-2-ylethanone has a molecular weight of 129.16 g/mol, XLogP of -0.44, 1 rotatable bonds, 1 hydrogen bond donors, and 3 hydrogen bond acceptors.
Where does this data come from?
All data for 1-morpholin-2-ylethanone is sourced from PubChem (CID 22263552), the world's largest open chemistry database maintained by the National Library of Medicine (NIH).