1221442-12-1 | 1-(3,5-Bis(trifluoromethyl)phenyl)-3-((1S,2S)-2-(dimethylamino)cyclohexyl)urea

Packsize	Purity	Availability	Price	Discounted Price
50mg	97%	in stock	$66.00	$47.00
100mg	97%	in stock	$106.00	$75.00
250mg	97%	in stock	$167.00	$117.00

Description

• Catalog Number: AA55336
• Chemical Name: 1-(3,5-Bis(trifluoromethyl)phenyl)-3-((1S,2S)-2-(dimethylamino)cyclohexyl)urea
• CAS Number: 1221442-12-1
• Molecular Formula: C17H21F6N3O
• Molecular Weight: 397.3586
• MDL Number: MFCD23380084
• SMILES: O=C(Nc1cc(cc(c1)C(F)(F)F)C(F)(F)F)N[C@H]1CCCC[C@@H]1N(C)C

Upstream Synthesis Route

The compound 1-(3,5-Bis(trifluoromethyl)phenyl)-3-((1S,2S)-2-(dimethylamino)cyclohexyl)urea, also known as $name$, plays a crucial role in chemical synthesis as a versatile reagent. Its unique structure combining a urea moiety with a bulky trifluoromethylphenyl group and a dimethylamino cyclohexyl group imparts special properties that make it valuable in various synthetic transformations.One significant application of $name$ in chemical synthesis is as a catalyst or reagent in asymmetric organic reactions. Due to the chiral centers present in the cyclohexyl moiety, $name$ can induce chirality in other molecules during chemical reactions, leading to the formation of enantiomerically enriched products. This feature is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals where enantiopurity is crucial for biological activity and effectiveness.Additionally, the trifluoromethylphenyl group in $name$ can serve as a directing group in organic reactions, facilitating selective functionalization of aromatic rings or enabling the construction of complex molecular architectures. This ability to control regioselectivity and chemoselectivity makes $name$ a valuable tool for the synthesis of a wide range of compounds with specific structural motifs.In summary, the compound $name$ is a versatile and powerful reagent in chemical synthesis, offering unique capabilities for inducing chirality, directing organic reactions, and enabling the construction of complex molecules with precision and efficiency. Its diverse applications make it an indispensable tool for synthetic chemists seeking to access new and challenging chemical space.