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C43H30F6NOP is a complex organic chemical compound characterized by its molecular formula that includes 43 carbon atoms, 30 hydrogen atoms, 6 fluorine atoms, 1 nitrogen atom, and 1 phosphorus atom. C43H30F6NOP likely possesses unique properties due to the presence of fluorine, nitrogen, and phosphorus atoms, which may contribute to its potential applications in various fields. Further analysis and testing are required to determine its specific identity and properties.

2011787-22-5

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2011787-22-5 Usage

Uses

Since the provided materials do not specify any particular uses for C43H30F6NOP, it is not possible to list its applications based on the given information. However, given its composition, it could potentially be used in various industries such as pharmaceuticals, materials science, or chemical research, depending on its properties once they are determined. If future research identifies specific applications, they could be listed as follows:
Used in Pharmaceutical Industry:
C43H30F6NOP could be used as a pharmaceutical agent for [specific medical application] due to [reason related to its chemical properties].
Used in Materials Science:
C43H30F6NOP could be employed as a material component in [specific material or product] for [reason related to its chemical properties].
Used in Chemical Research:
C43H30F6NOP might serve as a research compound for studying [specific area of chemistry or potential reactions] due to [reason related to its unique composition].

Check Digit Verification of cas no

The CAS Registry Mumber 2011787-22-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,1,1,7,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2011787-22:
(9*2)+(8*0)+(7*1)+(6*1)+(5*7)+(4*8)+(3*7)+(2*2)+(1*2)=125
125 % 10 = 5
So 2011787-22-5 is a valid CAS Registry Number.

2011787-22-5Downstream Products

2011787-22-5Relevant academic research and scientific papers

Phosphine-Catalyzed Asymmetric Umpolung Addition of Trifluoromethyl Ketimines to Morita–Baylis–Hillman Carbonates

Chen, Peng,Yue, Zhenting,Zhang, Junyou,Lv, Xi,Wang, Lei,Zhang, Junliang

, p. 13316 - 13320 (2016)

A novel phosphine-catalyzed, highly enantioselective umpolung addition of trifluoromethyl ketimines to Morita–Baylis–Hillman carbonates was developed and it provides facile access to optically active trifluoromethyl amines with a chiral tertiary stereocenter under mild reaction conditions. The salient features of this reaction include general substrate scope, mild reaction conditions, good yields, high enantioselectivity, ease of scale-up to gram scale, and further transformations of the products.

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