2126903-00-0 Usage
Description
(3aR,8aS)-2-(4-(trifluoromethyl)pyridin-2-yl)-8,8a-dihydro-3aH-indeno[1,2-d]oxazole is a complex heterocyclic compound featuring a trifluoromethyl group, a pyridine ring, and an oxazole ring fused together. It belongs to the class of dihydroindeno oxazoles, which are recognized for their potential pharmaceutical and biological activities. The intricate molecular structure, including the trifluoromethyl group and the heterocyclic rings, may enhance its reactivity and make it a promising candidate for various applications in medicinal chemistry. Further research is necessary to explore its full potential and properties.
Uses
Used in Pharmaceutical Industry:
(3aR,8aS)-2-(4-(trifluoromethyl)pyridin-2-yl)-8,8a-dihydro-3aH-indeno[1,2-d]oxazole is used as a potential pharmaceutical compound for its possible biological activities. The presence of the trifluoromethyl group and the heterocyclic rings may contribute to its reactivity and interaction with biological targets, making it a candidate for the development of new drugs.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (3aR,8aS)-2-(4-(trifluoromethyl)pyridin-2-yl)-8,8a-dihydro-3aH-indeno[1,2-d]oxazole is used as a subject of study to understand its properties, reactivity, and potential applications. (3aR,8aS)-2-(4-(trifluoromethyl)pyridin-2-yl)-8,8a-dihydro-3aH-indeno[1,2-d]oxazole's complex molecular structure and the presence of specific functional groups make it an interesting target for further investigation and development in the search for new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 2126903-00-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,1,2,6,9,0 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2126903-00:
(9*2)+(8*1)+(7*2)+(6*6)+(5*9)+(4*0)+(3*3)+(2*0)+(1*0)=130
130 % 10 = 0
So 2126903-00-0 is a valid CAS Registry Number.
2126903-00-0Relevant articles and documents
Enantioselective Construction of Trifluoromethoxylated Stereogenic Centers by a Nickel-Catalyzed Asymmetric Suzuki–Miyaura Coupling of Secondary Benzyl Bromides
Huang, Weichen,Wan, Xiaolong,Shen, Qilong
, p. 11986 - 11989 (2017)
Trifluoromethoxy-substituted stereogenic centers can be constructed with high enantioselectivity by a nickel-catalyzed Suzuki–Miyaura coupling of readily available α-bromobenzyl trifluoromethyl ethers with a variety of aryl pinacol boronates. The coupling proceeds under mild reaction conditions, and a variety of common functional groups, such as fluoride, chloride, bromide, ester, enolizable ketone, nitro, cyano, amino, and vinyl moieties, were well tolerated. Furthermore, the reaction can be easily scaled up to gram quantities without a decrease in enantioselectivity.
