Identification | Back Directory | [Name]
ICI-118,551 | [CAS]
72795-19-8 | [Synonyms]
Ici 111,581 ICI-118,551 ICI118551HCl ICI 118,551 HYDROCHLORIDE ICI 118551 Hydrochloride ((± ICI-118-551 HYDROCHLORIDE HIGHLY SELECTI VE B2 A Erythro-DL-1-(7-methylindan-4-yloxy)-3-isopropylaminobutan-2-ol erythro-DL-1-(7-Methylindan-4-yloxy)-3-isopropylamino-2-butanol (2R,3S)-rel-1-[(2,3-Dihydro-7-methyl-1H-inden-4-yl)oxy]-3-[(1-methylethyl)amino]-2-butanol 2-Butanol, 1-((2,3-dihydro-7-methyl-1H-inden-4-yl)oxy)-3-((1-methylethyl)amino)-, (2R,3S)-rel- 2-Butanol, 1-((2,3-dihydro-7-methyl-1H-inden-4-yl)oxy)-3-((1-methylethyl)amino)-, (R*,S*)-(+-)- (+/-)-1-[2,3-(DIHYDRO-7-METHYL-1H-INDEN-4-YL)OXY]-3-[(1-METHYLETHYL)AMINO]-2-BUTANOL HYDROCHLORIDE | [Molecular Formula]
C17H27NO2 | [MDL Number]
MFCD01074480 | [MOL File]
72795-19-8.mol | [Molecular Weight]
277.4 |
Chemical Properties | Back Directory | [Melting point ]
217-219°C | [storage temp. ]
Hygroscopic, -20°C Freezer, Under inert atmosphere | [solubility ]
ethanol: 7.3 mg/mL | [form ]
powder | [color ]
white |
Hazard Information | Back Directory | [Uses]
The (R,R)-enantiomer of ICI 118551 as highly selective β2-adrenoceptor antagonist. The S,S-enantiomer is the most potent. | [Definition]
ChEBI: ICI 118551 is an indane substituted at position 7 by a methyl group and at position 4 by a 3-(isopropylamino)-2-hydroxybutoxy group (the 2R,3S-diastereomer). It has a role as a beta-adrenergic antagonist. It is a member of indanes, an aromatic ether, a secondary alcohol and a secondary amino compound. |
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MOLEKULA Ltd.
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SIGMA-RBI
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