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1,3-Dioxane-4,6-dione, 2,2-dimethyl-5-[(1R)-1-(1-methylethyl)-3-phenyl-2-propynyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

862122-95-0

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862122-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862122-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,1,2 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 862122-95:
(8*8)+(7*6)+(6*2)+(5*1)+(4*2)+(3*2)+(2*9)+(1*5)=160
160 % 10 = 0
So 862122-95-0 is a valid CAS Registry Number.

862122-95-0Downstream Products

862122-95-0Relevant academic research and scientific papers

Monophosphine compound, transition metal complex thereof and production method of optically active compound using the complex as asymmetric catalyst

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Page/Page column 25-26, (2010/02/15)

The present invention provides a compound represented by the formula (I): wherein ring A is void or a benzene ring optionally having substituent(s), R1 and R2 are each independently a phenyl group optionally having substituent(s), a cyclohexyl group and the like, R3 and R4 are each independently a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group and the like, and X is a residue represented by —OR5 or —NHR6 wherein R5 and R6 are a lower alkyl group optionally having substituent(s), an aralkyl group optionally having substituent(s) and the like, a asymmetric transition metal complex containing the compound as a ligand and a production method of optically active compound using the complex as an asymmetric catalyst.

Catalytic, enantioselective, conjugate alkyne addition

Knoepfel, Thomas F.,Zarotti, Pablo,Ichikawa, Takashi,Carreira, Erick M.

, p. 9682 - 9683 (2007/10/03)

We document a copper-catalyzed, enantioselective, conjugate addition involving the direct use of a terminal acetylene, which undergoes in situ metalation. The addition reactions of phenylacetylene to Meldrum's acid derived acceptors take place in aqueous

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