Basic information
- CAS
102722-02-1- Standard SMILES
CC(C)(C)NCC(O)c1ccccc1O- InChIKey
FCEWRLVEPKVKBU-UHFFFAOYSA-N- Molecular formula
- C12H19NO2
- Average molar mass
- 209.28 g/mol
- Monoisotopic mass
- 209.14157885
Names & identifiers
- Preferred name
- D 2266
- IUPAC
- 2-[2-(tert-butylamino)-1-hydroxyethyl]phenol
- English name
- Benzenemethanol, alpha-(((1,1-dimethylethyl)amino)methyl)-2-hydroxy-, (+-)-
- Molecular weight
- 0
Names & synonyms
102722-02-1D 2266D-2266RefChem:9195352-[2-(tert-butylamino)-1-hydroxyethyl]phenolSCHEMBL8440055DTXSID50908022Benzenemethanol, alpha-[[(1,1-dimethylethyl)amino]methyl]-2-hydroxy-Benzenemethanol, alpha-(((1,1-dimethylethyl)amino)methyl)-2-hydroxy-, (+-)-
Database identifiers
- CAS
102722-02-1- PubChem CID
- 128191
- DTXSID
DTXSID50908022
Properties
Computed structural properties
- XLogP
- 1.8
- Topological polar surface area
- 52.5 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 4
- Heavy atoms
- 15
- Formal charge
- 0
- Complexity
- 189
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
Suppliers2 total
HONEST JOY HOLDINGS LIMITED[email protected]
CHEMICAL LAND21[email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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