(+)-4-[2-HYDROXY-3-[(1-METHYLETHYL)-AMINO]PROPOXY]BENZENEACETAMIDE

(+)-4-[2-HYDROXY-3-[(1-METHYLETHYL)-AMINO]PROPOXY]BENZENEACETAMIDE
  • CAS No.:56715-13-0
Other grades of this product :
(+)-4-[2-HYDROXY-3-[(1-METHYLETHYL)-AMINO]PROPOXY]BENZENEACETAMIDE Basic information
Product Name:(+)-4-[2-HYDROXY-3-[(1-METHYLETHYL)-AMINO]PROPOXY]BENZENEACETAMIDE
Synonyms:(R)-(+)-AtenololHCl;4-[(R)-2-Hydroxy-3-[(1-methylethyl)amino]propoxy]benzeneacetamide;2-[4-[(2R)-2-hydroxy-3-(isopropylamino)propoxy]phenyl]acetamide;2-[4-[(2R)-2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]acetamide;2-[4-[(2R)-2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]ethanamide;(R)-(+)-Atenolol,(+)-4-[2-Hydroxy-3-[(1-methylethyl)amino]propoxy]benzeneacetamide;R(+)-ATENOLOL LESS ACTIVE ENANTIOME;Benzeneacetamide, 4-[(2R)-2-hydroxy-3-[(1-methylethyl)amino]propoxy]-
CAS:56715-13-0
MF:C14H22N2O3
MW:266.34
EINECS:
Product Categories:Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:56715-13-0.mol
(+)-4-[2-HYDROXY-3-[(1-METHYLETHYL)-AMINO]PROPOXY]BENZENEACETAMIDE Chemical Properties
Melting point 148-152 °C(lit.)
Boiling point 508.0±50.0 °C(Predicted)
density 1.125±0.06 g/cm3(Predicted)
solubility 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: >6.0 mg/mL
pka13.88±0.20(Predicted)
form solid
color pale yellow
optical activity[α]25/D +16°, c = 1 in 1 M HCl
Safety Information
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
(+)-4-[2-HYDROXY-3-[(1-METHYLETHYL)-AMINO]PROPOXY]BENZENEACETAMIDE Usage And Synthesis
Description(+)-Atenolol is an enantiomer of the β1-adrenergic receptor (β1-AR) antagonist (±)-atenolol . (+)-Atenolol inhibits radioligand binding to β-ARs on sarcolemma-enriched membranes (Ki = 8.61 μM). Unlike (–)-atenolol and (±)-antenolol, (+)-atenolol has no effect on blood pressure in spontaneously hypertensive rats.
UsesCardioselective β-adrenergic blocker. Antihypertensive, antianginal, antiarrhythmic (class II).
UsesAntihypertensor
Usesless active enantiomer
DefinitionChEBI: The (R)-enantiomer of atenolol.
references[1] stoschitzky k, egginger g, zernig g, et al. stereoselective features of (r)- and (s)-atenolol: clinical pharmacological, pharmacokinetic, and radioligand binding studies[j]. chirality, 1993, 5(1): 15-19.
(+)-4-[2-HYDROXY-3-[(1-METHYLETHYL)-AMINO]PROPOXY]BENZENEACETAMIDE Preparation Products And Raw materials
Raw materialsAtenolol-->S(-)-ATENOLOL-->4-Hydroxyphenylacetamide-->4-Hydroxyphenylacetic acid-->Isopropylamine

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