ChemicalBook--->CAS DataBase List--->81732-46-9

81732-46-9

81732-46-9 Structure

81732-46-9 Structure
IdentificationMore
[Name]

Bambuterol hydrochloride
[CAS]

81732-46-9
[Synonyms]

BAMBEC
BAMBUTEROL HCL
BAMBUTEROL HYDROCHLORIDE
dimethylcarbamic acid 5-[2[(1,1-dimethyl)amino]1-hydroxyethyl]-1,3-phenylene ester hydrochloride
DIMETHYLCARBAMIC ACID 5-[2-[(1,1-DIMETHYLETHYL)AMINO]-1-HYDROXYETHYL]-1,3-PHENYLENE ESTER HYDROCHLORIDE
KWD-2183
Bambuterol monohydrochloride
BAMBUTEROL HYDROCHLORIDE, EP STANDARD
Dimethylcarbamic Acid 5-[2-(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,3-phenylene Ester, Hydrochloride, KWD-2183, Bambec,
Dimethylcarbmic acid 5-[2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,3-phenylene ester
[EINECS(EC#)]

643-060-9
[Molecular Formula]

C18H30ClN3O5
[MDL Number]

MFCD03427293
[Molecular Weight]

403.9
[MOL File]

81732-46-9.mol
Chemical PropertiesBack Directory
[Appearance]

White Solid
[Melting point ]

222-224°C
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

H2O: ~33 mg/mL, soluble
[form ]

powder
[color ]

off-white
[Usage]

Ester prodrug of the ?-adrenergic agonist terbutaline
[Merck ]

14,953
[InChIKey]

LBARATORRVNNQM-UHFFFAOYSA-N
[CAS DataBase Reference]

81732-46-9(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

24/25
[WGK Germany ]

3
[HS Code ]

29242990
Hazard InformationBack Directory
[Description]

Bambuterol is an inactive prodrug of terbutaline. It has a prolonged duration of action when administered orally.
[Chemical Properties]

White Solid
[Uses]

beta adrenergic agonist, bronchodilator, cholinesterase inhibitor
[Uses]

Ester prodrug of the ?2-adrenergic agonist terbutaline.
[Uses]

Ester prodrug of the ?-adrenergic agonist terbutaline
[Definition]

ChEBI: The hydrochloride salt of bambuterol. A long acting beta-adrenoceptor agonist used in the treatment of asthma, it is a prodrug for terbutaline.
[Synthesis]

Conventionally, as a method for preparing bambuterol hydrochloride, bis-3,5- (N, N-dimethylcarba) is subjected to an acylation process from 3 ′, 5′-dihydroxyacetophenone represented by the following reaction formula in US Pat. No. 4419364. Preparing moyloxy) -acetophenone (step 1); Preparing a bis-3 ′, 5 ′-(N, N-dimethylcarbamoyloxy) -2-bromo-acetophenone therefrom (step 2); Preparing an bis-3 ′, 5 ′-(N, N-dimethylcarbamoyloxy) -2- (N-benzyl tert-butyl) amino-acetophenone from the alkylation process therefrom (step 3); From this step to prepare a 1- [bis- (3 ', 5'-N, N-dimethylcarbamoyloxy) phenyl] -2-N-3 tert-butylaminoethanol hydrochloride, ie bambuterol hydrochloride.
Bambuterol hydrochloride
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

Bambuterol hydrochloride(81732-46-9)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

81732-46-9(sigmaaldrich)
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