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N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(1R,2R)-2-(1,3-dihydro-2H-isoindol-2-yl)cyclohexyl]-Thiourea is a thiourea derivative featuring a unique combination of substituent groups, including a phenyl and cyclohexyl group with fluorine atoms on the phenyl ring. This chemical compound is known for its thiourea functional group, which consists of a sulfur atom bonded to a nitrogen atom. Thioureas are widely used in organic synthesis and as ligands in metal-catalyzed reactions, and this specific compound may have potential applications in various fields such as pharmaceuticals, agrochemicals, or as a reagent in chemical research.

620960-27-2

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620960-27-2 Usage

Uses

Used in Pharmaceutical Industry:
N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(1R,2R)-2-(1,3-dihydro-2H-isoindol-2-yl)cyclohexyl]-Thiourea is used as a potential pharmaceutical candidate due to its unique structure and functional groups. Its ability to act as a ligand in metal-catalyzed reactions and its presence in organic synthesis processes make it a promising compound for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(1R,2R)-2-(1,3-dihydro-2H-isoindol-2-yl)cyclohexyl]-Thiourea may be utilized as a component in the development of new pesticides or herbicides. Its unique chemical structure could contribute to the creation of more effective and targeted agrochemical products.
Used in Chemical Research:
As a reagent in chemical research, N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(1R,2R)-2-(1,3-dihydro-2H-isoindol-2-yl)cyclohexyl]-Thiourea can be employed in various experimental setups and studies. Its properties and reactivity can be explored to gain insights into new chemical reactions and mechanisms, potentially leading to the discovery of novel compounds and applications.
However, it is important to note that further studies and research would be required to determine the specific properties, potential uses, and safety of N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(1R,2R)-2-(1,3-dihydro-2H-isoindol-2-yl)cyclohexyl]-Thiourea in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 620960-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,9,6 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 620960-27:
(8*6)+(7*2)+(6*0)+(5*9)+(4*6)+(3*0)+(2*2)+(1*7)=142
142 % 10 = 2
So 620960-27-2 is a valid CAS Registry Number.

620960-27-2Downstream Products

620960-27-2Relevant academic research and scientific papers

NEW PROCESS

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Page/Page column 64; 77; 78, (2017/06/02)

The present invention relates to a new chemical synthesis, intermediates and catalysts useful for the preparation of the neprilysin (NEP) inhibitor sacubitril. It further relates to new intermediate compounds and their use for said new chemical synthesis

Catalytic enantioselective iodoaminocyclization of hydrazones

Tripathi, Chandra Bhushan,Mukherjee, Santanu

supporting information, p. 3368 - 3371 (2014/07/08)

The first catalytic enantioselective iodoaminocyclization of β,γ-unsaturated hydrazones has been developed with the help of a trans-1,2-diaminocyclohexane-derived bifunctional thiourea catalyst and allows for the direct access to δ2-pyrazolines containing a quaternary stereogenic center in high yield with good enantioselectivity (up to 95% yield and 95:5 er).

ASYMMETRIC UREA COMPOUND AND PROCESS FOR PRODUCING ASYMMETRIC COMPOUND BY ASYMMETRIC CONJUGATE ADDITION REACTION WITH THE SAME AS CATALYST

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Page/Page column 14, (2008/06/13)

The present invention relates to a production method of asymmetric compound (IV) which includes conjugately adding nucleophilic reagent (III) to compound (II) in the presence of asymmetric urea compound (I). The present invention provides a non-metallic a

Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts

Okino, Tomotaka,Hoashi, Yasutaka,Takemoto, Yoshiji

, p. 12672 - 12673 (2007/10/03)

Michael reaction of malonates to nitroolefins with chiral bifunctional organocatalysts, bearing both a thiourea and tertiary amino group, afforded Michael adducts with high yields and enantioselectivities (up to 95%, up to 93% ee). Copyright

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