1162681-06-2 Usage
Description
4-methyl-N-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)benzenesulfonamide is a complex organic chemical compound characterized by the presence of a sulfonamide group attached to a benzene ring, which is in turn connected to a pyridine ring. Notably, this pyridine ring is adorned with a unique boron-containing dioxaborolane group. 4-methyl-N-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)benzenesulfonamide is recognized for its utility in the synthesis of more intricate molecular structures and holds promise in various scientific fields.
Uses
Used in Chemical Synthesis:
4-methyl-N-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)benzenesulfonamide serves as a valuable building block in chemical synthesis, facilitating the creation of a diverse array of complex organic molecules. Its unique structural features make it a versatile component in the assembly of novel chemical entities.
Used in Pharmaceutical Research:
In the realm of pharmaceutical research, this compound acts as an intermediate, playing a crucial role in the development of new drugs. Its incorporation into drug candidates can potentially enhance their efficacy, selectivity, or pharmacokinetic properties, contributing to the advancement of medicinal chemistry.
Used in Medicinal Chemistry for Drug Development:
4-methyl-N-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)benzenesulfonamide is utilized in medicinal chemistry for the design and synthesis of innovative pharmaceuticals. Its unique boron-containing group may offer specific binding affinities or reactivity that can be harnessed to create drugs with improved therapeutic profiles.
Used in Materials Science for Novel Material Creation:
Beyond its applications in synthesis and drug development, this compound also finds use in materials science. It contributes to the development of new materials with tailored properties, such as those with unique electronic, optical, or mechanical characteristics, by virtue of its structural components and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1162681-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,2,6,8 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1162681-06:
(9*1)+(8*1)+(7*6)+(6*2)+(5*6)+(4*8)+(3*1)+(2*0)+(1*6)=142
142 % 10 = 2
So 1162681-06-2 is a valid CAS Registry Number.
