2-[2-(tert-butylamino)-1-hydroxyethyl]phenol
-
![2-[2-(tert-butylamino)-1-hydroxyethyl]phenol structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/b42264d13f9b434494202dcaba429931.png "2-[2-(tert-butylamino)-1-hydroxyethyl]phenol")
2-[2-(tert-butylamino)-1-hydroxyethyl]phenol
structure -
-
CAS No:
102722-02-1
-
Formula:
C12H19NO2
-
Chemical Name:
2-[2-(tert-butylamino)-1-hydroxyethyl]phenol
-
Synonyms:
(+-)-alpha-(((2-hydroxy-1,1-dimethylethyl)amino)methyl)benzenemethanol;Benzenemethanol, alpha-(((1,1-dimethylethyl)amino)methyl)-2-hydroxy-, (+-)-;D 2266;D-2266;Dalgen;fepradinol;fepradinol hydrochloride;Flexidol;102722-02-1;2-[2-(tert-butylamino)-1-hydroxyethyl]phenol;D 2266;ACMC-1BPAY;D-2266;DTXSID50908022;Benzenemethanol, a-[[(1,1-dimethylethyl)amino]methyl]-2-hydroxy-;Benzenemethanol, alpha-(((1,1-dimethylethyl)amino)methyl)-2-hydroxy-, (+-)-
-
CAS No:
Drug Information
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. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)
(+-)-alpha-(((2-hydroxy-1,1-dimethylethyl)amino)methyl)benzenemethanol
Computed Properties
Molecular Weight:209.28
XLogP3:1.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:209.141578849
Monoisotopic Mass:209.141578849
Topological Polar Surface Area:52.5
Heavy Atom Count:15
Complexity:189
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Request for Quotation