530441-95-3 Usage
General Description
(R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethyl bromomethyl ether is a chemical compound with the molecular formula C11H9BrF12O. It is a highly fluorinated compound containing bromine and ether functional groups. (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethyl bromomethyl ether is often used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is known for its high reactivity and ability to undergo various chemical reactions, making it a versatile tool in the development of new organic compounds. Its unique structure and properties make it valuable in the field of medicinal chemistry and materials science, where its incorporation into molecular structures can impart desirable properties such as enhanced stability and bioactivity. However, it is important to handle this compound with caution due to its reactivity and potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 530441-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,0,4,4 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 530441-95:
(8*5)+(7*3)+(6*0)+(5*4)+(4*4)+(3*1)+(2*9)+(1*5)=123
123 % 10 = 3
So 530441-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9BrF6O/c1-6(19-5-12)7-2-8(10(13,14)15)4-9(3-7)11(16,17)18/h2-4,6H,5H2,1H3/t6-/m1/s1
530441-95-3Relevant articles and documents
Substituted heterocyclic compound as well as derivative, medicinal composition, preparation method and application thereof
-
Paragraph 0247; 0254; 0255; 0280, (2018/07/15)
The invention provides a substituted heterocyclic compound as well as a preparation method and application thereof, particularly a substituted heterocyclic compound as well as a derivative, a medicinal composition, a preparation method and application the
Asymmetric Synthesis of 4,4-Disubstituted-2-Imidazoli-dinones: Potent NK1 Antagonists
Reichard, Gregory A.,Stengone, Carmine,Paliwal, Sunil,Mergelsberg, Ingrid,Majmundar, Sapna,Wang, Cheng,Tiberi, Robert,McPhail, Andrew T.,Piwinski, John J.,Shih, Neng-Yang
, p. 4249 - 4251 (2007/10/03)
(Equation presented) A highly efficient and practical synthesis of 4,4-Disubstituted-2-Imidazolidinones utilizing a "self-reproduction of the center of chirality" strategy is described.