(R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone CAS 72332-33-3

Introduction:Basic information about (R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone CAS 72332-33-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone Basic information

Product Name:(R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone
Synonyms:(r*,s*)-(-)-8-hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1h)-quinolinone;PROCATEROL;2(1h)-quinolinone,8-hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-,(r*,;8-hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1h)-quinolinone(r*,s;s*)-(+-)-;ent-Florfenicol AMine-d3;(S)-N,N-DiMethyl-3-(1-naphthalenyl-d7-oxy)-3-(2-thienyl)propanaMine;ANTI-SARS VIRUS SM antibody produced in rabbit
CAS:72332-33-3
MF:C16H22N2O3
MW:290.36
EINECS:276-590-0
Product Categories:
Mol File:72332-33-3.mol

(R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone Chemical Properties

Melting point 107-109°C
storage temp. -20°C
solubility Acetonitrile (Slightly), Chloroform (Slightly), Methanol
form Solid
color White to Off-White
biological sourcerabbit
CAS DataBase Reference72332-33-3(CAS DataBase Reference)

Safety Information

Storage Class10 - Combustible liquids

(R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone Usage And Synthesis

DescriptionLike pirbuterol, procaterol exhibits similar broncholytic properties as albuteral, but it hassomewhat of a more prolonged action. It is recommended for use as an inhaled drug fortreating bronchial asthma.
Chemical PropertiesOff-White Solid
UsesA labelled intermediate of the enantiomer of Florfenicol (F405750), an antibacterial agent.
DefinitionChEBI: 8-hydroxy-5-[1-hydroxy-2-(propan-2-ylamino)butyl]-1H-quinolin-2-one is a member of quinolines.
Brand namePro-Air (Parke-Davis).
SynthesisProcaterol, 5-[1-hydroxy-2-[(1-methylethyl)amino]butyl]-8-hydroxy-2-(1H)quinolone (23.3.25), is synthesized by acylation of 8-hydroxy-2(1H)-quinolone with 2-bromobutyric acid chloride at the fifth position of the quinoline system, which gives thecompound 23.3.23. This undergoes action of isopropylamine, forming an aminoketone23.3.24, the carbonyl group of which is reduced by sodium borohydride, giving procaterol(23.3.25) .

(R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone Preparation Products And Raw materials

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