51461-11-1 Usage
Uses
Used in Pharmaceutical Industry:
N-(3-Amino-4-chlorophenyl)-4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butanamide is used as a pharmaceutical intermediate for the synthesis of various drugs and biologically active compounds. Its unique structure and functional groups contribute to the development of new therapeutic agents with specific pharmacological properties.
Used in Organic Synthesis:
In the field of organic synthesis, N-(3-Amino-4-chlorophenyl)-4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butanamide is utilized as a versatile building block. It can be incorporated into more complex organic molecules, facilitating the creation of novel chemical entities with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Drug Development:
N-(3-Amino-4-chlorophenyl)-4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butanamide is employed in drug development as a precursor for the synthesis of new pharmaceuticals. Its presence in the molecular structure can influence the pharmacokinetics, pharmacodynamics, and overall efficacy of the resulting drug candidates, making it a valuable component in the medicinal chemistry toolkit.
Used in Chemical Product Manufacturing:
Beyond its applications in the pharmaceutical sector, N-(3-Amino-4-chlorophenyl)-4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butanamide is also used in the manufacturing of various chemical products. Its unique chemical properties and reactivity make it suitable for the production of specialty chemicals, fine chemicals, and other high-value compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 51461-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,6 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51461-11:
(7*5)+(6*1)+(5*4)+(4*6)+(3*1)+(2*1)+(1*1)=91
91 % 10 = 1
So 51461-11-1 is a valid CAS Registry Number.
InChI:InChI=1/C26H37ClN2O2/c1-7-25(3,4)18-11-14-23(20(16-18)26(5,6)8-2)31-15-9-10-24(30)29-19-12-13-21(27)22(28)17-19/h11-14,16-17H,7-10,15,28H2,1-6H3,(H,29,30)
51461-11-1Relevant articles and documents
Catalytic liquid-phase reduction of aromatic nitro compounds containing highly reactive functional groups
Zhandarev,Kazin,Mironov
, p. 673 - 676 (2007/10/03)
Improved procedures have been proposed for fast and selective hydrogenation of aromatic nitro compounds with the goal of obtaining practically important amines.
