Basic information
- Standard SMILES
O=C1CCCCCCCCC1=O- InChIKey
HLPUHEJQIIHQDF-UHFFFAOYSA-N- Molecular formula
- C10H16O2
- Average molar mass
- 168.23 g/mol
- Monoisotopic mass
- 168.11502975
Names & identifiers
- Preferred name
- Sebacil
- IUPAC
- cyclodecane-1,2-dione
- English name
- Sebacile
- Molecular formula
- C10H16O2
- Molecular weight
- 0
Names & synonyms
Show more names
Database identifiers
- CAS
96-01-5- PubChem CID
- 96839
- DTXSID
DTXSID00242064- UNII
- 61P59MCH0P
- Nikkaji
- J4.717A
Properties
Computed structural properties
- XLogP
- 2.1
- Topological polar surface area
- 34.1 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 0
- Heavy atoms
- 12
- Formal charge
- 0
- Complexity
- 153
Physicochemical properties
- Melting point
- 40 · 40-41°
- Boiling point
- 18 · bp18 120-125°; bp10 104-105°
- Density
- 0.9812 · 0.9812 (rough estimate)
- refractive index
- 1.4578 · 1.4578 (estimate)
- FDA UNII
- 61 P59MCH0P · 61P59MCH0P
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Drugs that inhibit cholinesterases. The neurotransmitter ACETYLCHOLINE is rapidly hydrolyzed, and thereby inactivated, by cholinesterases. When cholinesterases are inhibited, the action of endogenously released acetylcholine at cholinergic synapses is potentiated. Cholinesterase inhibitors are widely used clinically for their potentiation of cholinergic inputs to the gastrointestinal tract and urinary bladder, the eye, and skeletal muscles; they are also used for their effects on the heart and the central nervous system.
Pesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics.
Uses & manufacturing
Suppliers1 total
Related reactions
Linked notes
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