100306-23-8 Usage
Uses
Used in Organic Synthesis:
(S)-2-bromo-1-(naphthalen-2-yl)ethanol is used as a reagent in organic synthesis for the preparation of chiral ligands and catalysts for asymmetric synthesis. Its chiral nature is crucial in creating enantiomerically pure compounds, which are essential in the pharmaceutical and agrochemical industries.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (S)-2-bromo-1-(naphthalen-2-yl)ethanol is used as a key intermediate in the production of various drugs. Its chiral properties allow for the creation of specific drug enantiomers, which can have different therapeutic effects and reduce the risk of side effects.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, (S)-2-bromo-1-(naphthalen-2-yl)ethanol is utilized for the synthesis of chiral pesticides and other agrochemicals. (S)-2-bromo-1-(naphthalen-2-yl)ethanol's ability to produce specific enantiomers helps in developing more effective and environmentally friendly products.
Used in Materials Science:
(S)-2-bromo-1-(naphthalen-2-yl)ethanol is also employed in the development of new materials for various industrial applications. Its unique structure contributes to the creation of materials with specific properties, such as improved stability or enhanced reactivity.
Used in Pharmacological Research:
(S)-2-bromo-1-(naphthalen-2-yl)ethanol has been studied for its potential pharmacological properties and biological activities. It shows promise as an anti-inflammatory and antifungal agent, which could lead to the development of new treatments for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 100306-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,0 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100306-23:
(8*1)+(7*0)+(6*0)+(5*3)+(4*0)+(3*6)+(2*2)+(1*3)=48
48 % 10 = 8
So 100306-23-8 is a valid CAS Registry Number.
100306-23-8Relevant academic research and scientific papers
Chiral guanidine catalyzed acylative kinetic resolution of racemic 2-bromo-1-arylethanols
Sawada, Erika,Nakata, Kenya
supporting information, p. 371 - 373 (2021/03/16)
In this study, chiral guanidine catalyzed acylative kinetic resolution of racemic 2-bromo-1-arylethanols was achieved with high selectivity. Irrespective of the electronic nature and the substitution patterns on the aromatic rings, a variety of substrates were suitable for this reaction. The branched acyl component was considered to be optimal for obtaining high s-values. The transition state of the reaction was proposed based on the absolute configuration of the obtained product.
