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54063-54-6

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54063-54-6 Usage

Description

Reproterol, also known as Reproterol Hydrochloride, is a synthetic medication belonging to the class of β2 adrenoceptor agonists. It is an off-white solid with chemical properties that allow it to interact with specific receptors in the body, leading to its therapeutic effects. Reproterol is primarily used for treating respiratory conditions, particularly asthma, by promoting bronchodilation and reducing inflammation.

Uses

Used in Pharmaceutical Industry:
Reproterol is used as a bronchodilator for the treatment of asthma. It works by stimulating β2 adrenoceptors in the lungs, leading to the relaxation of smooth muscle cells and subsequent widening of the airways. This helps alleviate the symptoms of asthma, such as shortness of breath, wheezing, and coughing.
Additionally, Reproterol may be used in other respiratory conditions where bronchodilation is required, such as chronic obstructive pulmonary disease (COPD) and exercise-induced asthma. However, it is important to note that the use of Reproterol should be under the guidance of a healthcare professional, as it may have potential side effects and contraindications.

Check Digit Verification of cas no

The CAS Registry Mumber 54063-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,6 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54063-54:
(7*5)+(6*4)+(5*0)+(4*6)+(3*3)+(2*5)+(1*4)=106
106 % 10 = 6
So 54063-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H23N5O5/c1-21-16-15(17(27)22(2)18(21)28)23(10-20-16)5-3-4-19-9-14(26)11-6-12(24)8-13(25)7-11/h6-8,10,14,19,24-26H,3-5,9H2,1-2H3

54063-54-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-[3-[[2-(3,5-dihydroxyphenyl)-2-hydroxyethyl]amino]propyl]-1,3-dimethylpurine-2,6-dione

1.2 Other means of identification

Product number -
Other names Reproterol [INN:BAN]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54063-54-6 SDS

54063-54-6Upstream product

54063-54-6Downstream Products

54063-54-6Relevant articles and documents

Combined doses

-

, (2008/06/13)

The present invention discloses a method and a pharmaceutical dry powder combined dose for the prophylaxis or treatment of a respiratory disorder in a mammalian host by inhalation of a metered dry powder combined dose of finely divided dry medication powders. At least one dry powder medicament is selected from a first group of bronchodilating medicaments and at least one dry powder medicament from a second group of anti-inflammatory medicaments. A metered dry powder medicinal combined dose comprising separately metered deposits of medicinally suitable quantities of each of the selected medicaments is prepared, in which the sum of the metered deposits constitutes the metered quantities of powder of the combined dose and the medicinal combined dose is introduced into an adapted inhaler device for a generally simultaneous delivery of the medicinal combined dose during the course of a single inhalation by a user, such that the delivered medicinal combined dose is composed of a high proportion of mixed de-aggregated fine particles of the selected medicaments, whereby an desired therapeutic or treating effect to the user is achieved.

Synthesis of bronchospasmolytically effective β phenylethyl aminoalkyl xanthines

Klingler

, p. 4 - 14 (2007/10/05)

New theophylline and theobromine derivatives are synthesized from the β phenylethylaminoalkyl xanthines, whose phenyl substituent is substituted by one or two hydroxyl groups and partially also by other substituents. Different methods of synthesis are described, among them the production of the bronchospasmolytic 7 (3 [2 (3,5 dihydroxyphenyl) 2 hydroxy ethylamino] propyl) theophylline (reproterol . HCl).

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