1160186-73-1 Usage
Uses
Used in Organic Synthesis:
Potassium (3-aminophenyl)trifluoroboranuide is used as a reagent for the formation of carbon-carbon and carbon-nitrogen bonds, which are crucial in the synthesis of various organic compounds. Its reactivity and stability make it a valuable tool in synthetic chemistry for creating complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Potassium (3-aminophenyl)trifluoroboranuide is utilized as a key intermediate in the synthesis of certain pharmaceutical compounds. Its ability to form carbon-carbon and carbon-nitrogen bonds is essential for constructing the molecular frameworks of various drugs.
Used in Chemical Research:
In the field of chemical research, Potassium (3-aminophenyl)trifluoroboranuide serves as a versatile reagent for exploring new reaction pathways and mechanisms. Its unique properties allow researchers to investigate novel synthetic methods and develop innovative approaches to chemical bond formation.
Used in Material Science:
In material science, Potassium (3-aminophenyl)trifluoroboranuide is employed in the development of new materials with specific properties. Its role in forming carbon-carbon and carbon-nitrogen bonds can contribute to the creation of advanced polymers, composites, and other materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1160186-73-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,1,8 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1160186-73:
(9*1)+(8*1)+(7*6)+(6*0)+(5*1)+(4*8)+(3*6)+(2*7)+(1*3)=131
131 % 10 = 1
So 1160186-73-1 is a valid CAS Registry Number.
1160186-73-1Relevant articles and documents
Preparation of organotrifluoroborate salts: Precipitation-driven equilibrium under non-etching conditions
Lennox, Alastair J. J.,Lloyd-Jones, Guy C.
supporting information, p. 9385 - 9388 (2012/10/29)
Simple, rapid, and scaleable: In contrast to current procedures using corrosive HF/MF or MHF2 reagents (M=e.g. K), a wide range of trifluoroborates can be rapidly, simply, and safely prepared from MF (M=K, Cs), RCO2H, and a boronic a
