4745-77-1 Usage
Description
2-[(2,4-difluorophenyl)amino]-4-methyl-4,5-dihydro-1,3-thiazol-4-ylmethanol is a synthetic compound characterized by a complex molecular structure that features a thiazole ring, a methyl group, a difluorophenyl amino group, and a methanol moiety. The presence of these functional groups indicates potential biological and pharmacological properties, making it a candidate for various applications in the field of medicinal chemistry.
Uses
Used in Pharmaceutical Development:
2-[(2,4-difluorophenyl)amino]-4-methyl-4,5-dihydro-1,3-thiazol-4-ylmethanol is used as a building block or a core structure in the development of pharmaceuticals targeting thiazole-containing receptors or enzymes. Its unique molecular composition allows for the potential modulation of various biological pathways and interactions with specific cellular targets.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-[(2,4-difluorophenyl)amino]-4-methyl-4,5-dihydro-1,3-thiazol-4-ylmethanol serves as a valuable compound for research purposes. It can be used to study the structure-activity relationships of thiazole-containing drugs and to develop new therapeutic agents with improved efficacy and selectivity.
Used in Drug Design and Optimization:
2-[(2,4-difluorophenyl)amino]-4-methyl-4,5-dihydro-1,3-thiazol-4-ylmethanol can be employed in drug design and optimization processes, where its unique structural features can be leveraged to create novel therapeutic agents with enhanced pharmacokinetic and pharmacodynamic properties. Its potential applications may include the treatment of various diseases and conditions, pending further research and development.
Used in Chemical Synthesis:
2-[(2,4-difluorophenyl)amino]-4-methyl-4,5-dihydro-1,3-thiazol-4-ylmethanol can also be utilized as an intermediate or a reagent in the synthesis of other complex organic molecules, particularly those with potential applications in the pharmaceutical, agrochemical, or materials science industries.
Check Digit Verification of cas no
The CAS Registry Mumber 4745-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,4 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4745-77:
(6*4)+(5*7)+(4*4)+(3*5)+(2*7)+(1*7)=111
111 % 10 = 1
So 4745-77-1 is a valid CAS Registry Number.
4745-77-1Relevant articles and documents
Palladium(0)-catalyzed dearomative arylation of indoles: Convenient access to spiroindolenine derivatives
Wu, Ke-Jia,Dai, Li-Xin,You, Shu-Li
, p. 3772 - 3775 (2012/08/29)
Dearomatization of an indole via palladium(0)-catalyzed cross-coupling reaction has been realized. With readily available triphenylphosphine as ligand, various spiroindolenine derivatives have been obtained in good to excellent yields, and enantioselectiv
