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578-84-7
7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one

Catalog#:1P003NWM

CAS:578-84-7

MDL:MFCD00760804

Molecular Formula:C11H7F3O3

Molecular Weight:244.1667

UN Number:

Haz Class:

Packing Group:

Synonyms: 7-methoxy-2-(trifluoromethyl)-4H-chromen-4-one; 578-84-7; DivK1c_005142; CTK1E0617; DTXSID00357920; WT870; ZINC437880; BDBM50444536; CCG-10914; MFCD00760804; STK074790; AKOS001704383; CHEMBL3099591; DS-6436; MCULE-9210328196; KS-000001A4; AJ-22868; BIM-0023812.P001; 7-methoxy-2-(trifluoromethyl)chromen-4-one; AX8220957; ST24045683; X5672; Q-9355; 7-methoxy-2-trifluoromethylchromone; SR-01000513684; SR-01000513684-1; 2-(Trifluoromethyl)-7-methoxy-4H-1-benzopyran-4-one; A1154/0053983; 578-84-7 7-methoxy-2-(trifluoromethyl)-4H-chromen-4-one; C11H7F3O3; CID871502; 2-(trifluoromethyl)-7-methoxy-4H-chromen-4-one; 4H-1-Benzopyran-4-one, 7-methoxy-2-(trifluoromethyl)-; AK114291; CDS1_004102; AC1LHYN6; CBMicro_023686; MixCom6_000710;

Keywords: 578-84-7,MFCD00760804,1P003NWM,7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one,C11H7F3O3

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P003NWM 97% 250mg $180.00 $135.00 In Stock USA ADD TO CART BUY NOW
1P003NWM 97% 1g $314.00 $235.00 In Stock USA ADD TO CART BUY NOW 

  • 7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one is a versatile chemical compound widely utilized in chemical synthesis as a key building block. Its unique structure containing a trifluoromethyl group and a chromenone moiety lends itself to various synthetic pathways for the preparation of complex organic molecules with diverse functionalities.In organic synthesis, 7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one serves as a valuable intermediate for the construction of bioactive compounds, pharmaceuticals, and agrochemicals. The trifluoromethyl group enhances the compound's lipophilicity and metabolic stability, making it a valuable component in drug design and discovery. Additionally, the chromenone scaffold offers a versatile platform for further functionalization through various chemical reactions such as nucleophilic substitutions, condensations, and cyclizations.Moreover, the presence of the methoxy group provides an opportunity for selective modifications, enabling the fine-tuning of the compound's properties for specific applications. Overall, the strategic incorporation of 7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one in chemical synthesis enables the efficient synthesis of complex molecules with enhanced biological activities and potential therapeutic benefits.

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