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1,3-BIS-(ALPHA,ALPHA,ALPHA,ALPHAPR,ALPHAPR,ALPHAPR-HEXAFLUORO-3,5-XYLYL)-UREA

Names

[ CAS No. ]:
3824-74-6

[ Name ]:
1,3-BIS-(ALPHA,ALPHA,ALPHA,ALPHAPR,ALPHAPR,ALPHAPR-HEXAFLUORO-3,5-XYLYL)-UREA

[Synonym ]:
Urea,N,N'-bis[3,5-bis(trifluoromethyl)phenyl]
3,3',5,5'-tetrakis(trifluoromethyl)carbanilide
1,3-bis(3,5-bis(trifluoromethyl)phenyl)urea
N,N'-di[3,5-di(trifluoromethyl)phenyl]urea
N,N'-Bis-<3,5-bis(trifluormethyl)-phenyl>-harnstoff
N-[3,5-Bis(trifluoromethyl)phenyl]{[3,5-bis(trifluoromethyl)phenyl]amino}carboxamide
[bis(3,5-trifluoromethyl)benzene]urea

Chemical & Physical Properties

[ Molecular Formula ]:
C17H8F12N2O

[ Molecular Weight ]:
484.23900

[ Exact Mass ]:
484.04500

[ PSA ]:
44.62000

[ LogP ]:
7.49240

MSDS

Safety Information

[ RIDADR ]:
NONH for all modes of transport

Synthetic Route

Precursor & DownStream

Articles

Urea derivatives are highly active catalysts for the base-mediated generation of terminal epoxides from aldehydes and trimethylsulfonium iodide.

Org. Biomol. Chem. 6(8) , 1339-43, (2008)

N,N'-Diarylureas have been shown to efficiently catalyse sulfonium ylide-mediated aldehyde epoxidation reactions for the first time. These processes are of broad scope and can be coupled with a subseq...

Internal Lewis acid assisted hydrogen bond donor catalysis.

Org. Lett. 13(4) , 716-9, (2011)

Boronate ureas are introduced as a new class of noncovalent catalysts for conjugate addition reactions with enhanced activity. Through intramolecular coordination of the urea functionality to a strate...

Bonding Organocatalysed Friedel-Crafts Alkylation of Aromatic and Heteroaromatic Systems with Nitroolefins Dessole G,et al.

Synlett 13 , 2374-2378, (2004)


More Articles


Related Compounds

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