215317-11-6 Usage
Description
(R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol is a complex chiral molecule with a long carbon chain and an alcohol functional group at one end, coupled with a sophisticated aromatic structure at the other end. (R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol is characterized by its (R) designation, indicating a specific spatial orientation. It features a phenylethyl group, a phenoxy group, and a phenyl group, all contributing to its aromatic properties. The combination of two bulky aromatic groups and a long carbon chain endows this molecule with a high level of complexity and potential biological activity, making it a candidate for various applications in the fields of pharmaceuticals and organic synthesis.
Uses
Used in Pharmaceutical Industry:
(R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol is used as a potential active pharmaceutical ingredient due to its complex structure and chirality, which may offer unique interactions with biological targets and contribute to the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol can be utilized as a building block or intermediate for the creation of more complex molecules with specific functions or properties, taking advantage of its aromatic and chiral characteristics.
Used in Chiral Chemistry:
The chirality of (R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol makes it a valuable compound in chiral chemistry, where it can be employed in the synthesis of enantiomerically pure compounds, which are essential in various applications, including pharmaceuticals and agrochemicals.
Used in Fragrance Industry:
Given its aromatic nature, (R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol may also find applications in the fragrance industry, where it could be used to create novel scents or enhance existing ones.
Used in Material Science:
The unique structure of (R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol could potentially be exploited in material science for the development of new materials with specific properties, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 215317-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,3,1 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 215317-11:
(8*2)+(7*1)+(6*5)+(5*3)+(4*1)+(3*7)+(2*1)+(1*1)=96
96 % 10 = 6
So 215317-11-6 is a valid CAS Registry Number.
215317-11-6Relevant articles and documents
Process to produce a protease inhibitor
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, (2008/06/13)
Disclosed is a novel process and novel intermediates to prepare [R-(R*,R*)]-N-[3-[1-[5,6-dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide (XIX) which is a protease inhibitor useful in treating humans infected with the HIV virus.
