406920-63-6 Usage
Description
(3R)-3-(1-METHYL-1H-INDOL-3-YL)-3-PHENY, with the molecular formula C21H19N, is a chiral molecule characterized by its non-superposable mirror image. (3R)-3-(1-METHYL-1H-INDOL-3-YL)-3-PHENY features a phenyl group and a 1-methyl-1H-indol-3-yl group connected to a central carbon atom via single bonds. Its unique structure and properties make it a promising candidate for pharmaceuticals and organic synthesis, although further research is needed to explore its full potential.
Uses
Used in Pharmaceutical Industry:
(3R)-3-(1-METHYL-1H-INDOL-3-YL)-3-PHENY is used as a chiral building block for the development of pharmaceutical compounds. Its unique structure allows it to be a key component in the synthesis of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (3R)-3-(1-METHYL-1H-INDOL-3-YL)-3-PHENY serves as a valuable intermediate for the creation of various organic compounds. Its distinct properties enable it to be a versatile component in the synthesis of a wide range of molecules with different applications.
More research is necessary to fully understand the potential uses and effects of (3R)-3-(1-METHYL-1H-INDOL-3-YL)-3-PHENY, as its unique structure and properties may lead to new discoveries and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 406920-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,9,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 406920-63:
(8*4)+(7*0)+(6*6)+(5*9)+(4*2)+(3*0)+(2*6)+(1*3)=136
136 % 10 = 6
So 406920-63-6 is a valid CAS Registry Number.
406920-63-6Relevant articles and documents
Mapping the Surface Groups of Amine-Rich Carbon Dots Enables Covalent Catalysis in Aqueous Media
Amato, Francesco,Bonchio, Marcella,Companyó, Xavier,Dell'Amico, Luca,Filippini, Giacomo,Prato, Maurizio,Ragazzon, Giulio,Rosso, Cristian,Vega-Pe?aloza, Alberto
supporting information, p. 3022 - 3037 (2020/11/03)
Carbon nanodots stand as the missing link between the molecular and the nanoscale world, owing to the unique molecular-like behavior emerging from their synthetic precursors. A converging set of analytical and spectroscopic data yields a precise inventory
Alkyne Hydroheteroarylation: Enantioselective Coupling of Indoles and Alkynes via Rh-Hydride Catalysis
Cruz, Faben A.,Zhu, Yamin,Tercenio, Quentin D.,Shen, Zengming,Dong, Vy M.
, p. 10641 - 10644 (2017/08/15)
We report an enantioselective coupling between alkynes and indoles. A Rh-hydride catalyst isomerizes alkynes to generate a metal-allyl species that can be trapped with both aromatic and heteroaromatic nucleophiles.
Hydrogen-bond-mediated supramolecular iminium ion catalysis
Wang, Yao,Yu, Tian-Yang,Zhang, Hong-Bo,Luo, Yong-Chun,Xu, Peng-Fei
supporting information, p. 12339 - 12342 (2013/02/23)
Mod squad: Multiple small molecules appear to spontaneously self-assemble to form supramolecular amine catalysts that have high reactivity, good efficiency, and enhanced turnover numbers. These modular organocatalysts should be applicable to many iminium as well as hydrogen-bond catalytic reactions and provide new insights into asymmetric catalysis. Copyright
