1260955-10-9 Usage
Uses
Used in Chemical Synthesis:
(RS)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanamine is used as a building block for the synthesis of other organic compounds. Its unique structure, which includes a boron atom and a phenyl group, allows it to participate in a range of chemical reactions, facilitating the creation of diverse molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (RS)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanamine is used as an intermediate in the development of new drugs. Its chiral nature and structural versatility make it a valuable component in the design and synthesis of novel pharmaceutical compounds, potentially leading to the discovery of new treatments for various medical conditions.
Used in Material Science:
(RS)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanamine is also utilized in material science for the development of new materials with specific properties. Its ability to form various chemical bonds and its structural characteristics make it a promising candidate for the creation of advanced materials with applications in electronics, coatings, and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1260955-10-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,9,5 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1260955-10:
(9*1)+(8*2)+(7*6)+(6*0)+(5*9)+(4*5)+(3*5)+(2*1)+(1*0)=149
149 % 10 = 9
So 1260955-10-9 is a valid CAS Registry Number.
1260955-10-9Relevant academic research and scientific papers
Chemoenzymatic synthesis of boron-containing chiral amines and amides
Andrade, Leandro H.,Barcellos, Thiago,Santiago, Carolina G.
experimental part, p. 2419 - 2424 (2010/12/25)
The first application of lipases as catalysts to obtain optically active boron-containing amines and amides is described. We studied several reaction conditions to achieve the kinetic resolution of boron-containing amines via enantioselective acylation me
