Colterol | |
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Salts [] | |
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Colterol mesylate | |
Esters [] | |
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Colterol acetate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C12H19NO3 |
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Molecular mass | 225.28 g/mol |
Predicted LogP | -0.4 |
Chirality | racemic |
Identifiers [] | |
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IUPAC name | 4-[2-(tert-butylamino)-1-hydroxyethyl]benzene-1,2-diol |
SMILES | CC(C)(C)NCC(C1=CC(=C(C=C1)O)O)O |
InChI | InChI=1S/C12H19NO3/c1-12(2,3)13-7-11(16)8-4-5-9(14)10(15)6-8/h4-6,11,13-16H,7H2,1-3H3 |
InChIKey | PHSMOUBHYUFTDM-UHFFFAOYSA-N |
Dosing |
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Colterol
(Redirected from (-)-Colterol)
Colterol (also known as Colterolum, (+-)-N-tert-Butylarterenol, (+-)-N-t-Butylnoradrenaline, dl-N-tert-Butylnorepinephrine, (+-)-tert-Butyl noradrenaline, KWD 2026, WIN-5563, S 1541, S-1541 or dl-1-(3,4-Dihydroxyphenyl)-2-tert-butylaminoethanol) is a sympathomimetic substance of the phenylethanolamine class.
Chemistry
Colterol is typically found in the form of its mesylate salt or its acetate ester.
Stereochemistry
(RS)-Colterol is a racemic mixture of the optical stereoisomers:Stereoisomers [] | |
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(+)-Colterol | (-)-Colterol |