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CAS

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894079-56-2

3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride, with the molecular formula C11H17NO.HCl, is a hydrochloride salt form of 3-((S)-1-DiMethylaMino-ethyl)phenol. It is a selective beta-adrenergic agonist that functions as a bronchodilator, relaxing the muscles in the airways to facilitate easier breathing.

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  • 894079-56-2 Structure

  • Basic information

    1. Product Name: 3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride
    2. Synonyms: 3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride;(S)-3-1-(Dimethylamino)ethylphenol hydrochloride;3-[(1S)-1-(Dimethylaminoethyl)]phenol hydrochloride
    3. CAS NO:894079-56-2
    4. Molecular Formula: C10H15NO*ClH
    5. Molecular Weight: 201.69314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 894079-56-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride(894079-56-2)
    11. EPA Substance Registry System: 3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride(894079-56-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 894079-56-2(Hazardous Substances Data)

894079-56-2 Usage

Uses

Used in Pharmaceutical Industry:
3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride is used as a bronchodilator for the treatment of respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its selective action on beta-adrenergic receptors helps alleviate symptoms by relaxing the airway muscles, improving airflow.
Used in Respiratory Therapy:
3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride is used as a therapeutic agent in respiratory therapy to manage and alleviate symptoms of asthma and COPD. Its bronchodilating effect provides relief to patients experiencing breathing difficulties.
Used in Inhalation Therapy:
3-((S)-1-DiMethylaMino-ethyl)phenol hydrochloride is used in inhalation therapy, where it is administered through inhalers and nebulizers. The hydrochloride form enhances the stability and solubility of the compound, making it suitable for pharmaceutical applications and ensuring effective delivery to the target site in the respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 894079-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,0,7 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 894079-56:
(8*8)+(7*9)+(6*4)+(5*0)+(4*7)+(3*9)+(2*5)+(1*6)=222
222 % 10 = 2
So 894079-56-2 is a valid CAS Registry Number.

894079-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(1S)-1-(dimethylamino)ethyl]phenol,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:894079-56-2 SDS

894079-56-2Relevant articles and documents

SYNTHETIC METHOD OF PHENYLCARBAMATE DERIVATIVE

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Page/Page column 4-5, (2008/06/13)

Disclosed herein is a method for synthesizing the compound of Formula 1 or an acid addition salt thereof: The method comprises the steps of subjecting the compound of Formula 7 to N-methylation to obtain the compound of Formula 8 or an acid addition salt thereof: and subjecting the compound of Formula 8 or an acid addition salt thereof to O-carbamoylation to obtain the compound of Formula 1 or an acid addition salt thereof.

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