61241-54-1 Usage
Chemical family
Inden-1-one derivatives The compound belongs to the family of inden-1-one derivatives, which are synthetic organic compounds.
Physical appearance
Pale-yellow solid The chemical compound appears as a pale-yellow solid in its pure form.
Solubility
Insoluble in water, soluble in organic solvents The compound does not dissolve well in water but dissolves easily in organic solvents, such as ethanol or acetone.
Industrial use
Synthesis of various drugs 1H-Inden-1-one, 5-fluoro-2,3-dihydro-3-methyl is used in the pharmaceutical industry to create a variety of drugs.
Chemical reagent
Reagent in chemical reactions The compound serves as a reagent in various chemical reactions, aiding in the formation of new molecules.
Research and development
Building block for new molecules The compound has potential applications in research and development, as it can be used as a building block for creating new molecules with diverse biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 61241-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61241-54:
(7*6)+(6*1)+(5*2)+(4*4)+(3*1)+(2*5)+(1*4)=91
91 % 10 = 1
So 61241-54-1 is a valid CAS Registry Number.
61241-54-1Relevant articles and documents
Asymmetric Induction in Hydroacylation by Cooperative Iminium Ion-Transition-Metal Catalysis
Rastelli, Ettore J.,Truong, Ngoc T.,Coltart, Don M.
, p. 5588 - 5591 (2016)
A new strategy for the rhodium-catalyzed enantioselective hydroacylation is described. This has been achieved through the merger of iminium ion catalysis and transition-metal catalysis such that asymmetric induction derives from a readily accessible, inexpensive chiral nonracemic secondary amine catalyst rather than a chiral nonracemic phosphine as is typical of conventional asymmetric hydroacylation methods.
