380225-68-3 Usage
Uses
Used in Organic Chemical Synthesis:
1-(2-bromo-6-methoxy-phenyl)ethanone is used as a building block for the synthesis of various organic compounds. The presence of the bromine and methoxy groups allows for selective reactions and functionalization, making it a versatile intermediate in the preparation of complex organic molecules.
Used in Pharmaceutical Research:
1-(2-bromo-6-methoxy-phenyl)ethanone is used as a reagent in pharmaceutical research for the development of new drugs. Its unique structure and reactivity can be exploited to create novel drug candidates with potential therapeutic applications.
Used in Chemical Applications:
1-(2-bromo-6-methoxy-phenyl)ethanone is used as a reagent in various chemical applications due to its specific properties and reactivity imparted by the bromine and methoxy groups. This allows for its use in the synthesis of compounds with tailored properties for specific applications in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 380225-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,2,2 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 380225-68:
(8*3)+(7*8)+(6*0)+(5*2)+(4*2)+(3*5)+(2*6)+(1*8)=133
133 % 10 = 3
So 380225-68-3 is a valid CAS Registry Number.
380225-68-3Relevant academic research and scientific papers
Asymmetric Synthesis and Application of Chiral Spirosilabiindanes
Chang, Xin,Chen, Hong-Chao,Li, Chuan-Ying,Ma, Pei-Long,Wang, Peng
supporting information, p. 8937 - 8940 (2020/04/30)
Reported here is the development of a class of chiral spirosilabiindane scaffolds by Rh-catalyzed asymmetric double hydrosilation, for the first time. Enantiopure SPSiOL (spirosilabiindane diol), a new type of chiral building block for the preparation of various chiral ligands and catalysts, was readily prepared on greater than 10 gram scale using this protocol. The potential of this new spirosilabiindane scaffold in asymmetric catalysis was preliminarily demonstrated by development of the corresponding monodentate phosphoramidite ligands (SPSiPhos), which were used in both a Rh-catalyzed hydrogenation and a Pd-catalyzed intramolecular carboamination.
A novel palladium-catalyzed domino Tsuji - Trost - Heck process for the synthesis of tetrahydroanthracenes
Tietze, Lutz F.,Nordmann, Gero
, p. 3247 - 3253 (2007/10/03)
A novel type of palladium-catalyzed domino reaction is described combining Tsuji - Trost and Heck reactions. This method allows efficient access to tetrahydroanthracene derivatives 1 in up to 89% isolated yield in a one-pot process starting from the diket
