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63918-85-4 Usage

Type of compound

Amino alcohol

Key functional group


Commonly found in

Certain medications and dietary supplements

Potential use


Potential use

Beta-adrenergic agonist

Possible properties


Studied for treatment of

Respiratory conditions (e.g. asthma, COPD)

Investigated for

Enhancing athletic performance

Investigated for

Promoting weight loss

Need for further research

To understand pharmacological properties and therapeutic uses

Check Digit Verification of cas no

The CAS Registry Mumber 63918-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,1 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63918-85:
154 % 10 = 4
So 63918-85-4 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name 2-(1-phenylpropan-2-ylamino)ethanol

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:63918-85-4 SDS

63918-85-4Relevant articles and documents

Efficient preparation of secondary aminoalcohols through a Ti(IV) reductive amination procedure. Application to the synthesis and antibacterial evaluation of new 3β-N-[hydroxyalkyl]aminosteroid derivatives

Salmi, Chanaz,Loncle, Céline,Letourneux, Yves,Brunel, Jean Michel

, p. 4453 - 4459 (2008/09/20)

An efficient method for the synthesis of various secondary aminoalcohols through a titanium(IV) isopropoxide-mediated reductive amination reaction of ketones is reported. Thus, different ketones gave the expected products in moderate to excellent yields up to 89% in numerous cases. A series of 3β-N-[hydroxyalkyl]aminosteroid derivatives were prepared according to this methodology and evaluated for their in vitro antimicrobial properties against human pathogens. All the compounds showed moderate to excellent activities against Gram-positive bacteria exhibiting similar results against Staphylococcus aureus and Streptococcus faecalis with Minimum Inhibitory Concentrations (MICs) varying from 3.12 to 25 μg/mL. No significant antibacterial activities are encountered against Gram-negative bacteria.

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