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654-99-9
5-Fluoro-2-(trifluoromethyl)benzoic acid

Catalog#:1P003N77

CAS:654-99-9

MDL:MFCD18208176

Molecular Formula:C8H4F4O2

Molecular Weight:208.1098

UN Number:

Haz Class:

Packing Group:

Synonyms: 5-Fluoro-2-(trifluoromethyl)benzoic acid; 654-99-9; ACMC-209wv9; KSC495K4F; AKOS AKM01163; SCHEMBL222474; RARECHEM AL BO 0853; CTK3J5542; ZINC57043; DTXSID90350864; BRFNBGWEOKQIND-UHFFFAOYSA-N; WT081; 2-trifluoromethyl-5-fluorobenzoic acid; AC1Q7230; ACT12059; JRD-0747; KS-00000M4B; ANW-46867; CF-941; SBB064470; AKOS005067841; 3-Fluoro-6-trifluoromethylbenzoic acid; AC-3994; 5-fluoro-2-trifluoromethylbenzoic acid; AM84155; AS01889; CM12800; CS-W023084; MCULE-4745532087; RP26400; RTR-022286; 5-fluoro 2-trifluoromethyl benzoic acid; 5-fluoro-2-trifluoromethyl benzoic acid; 5-fluoro-2-trifluoromethyl-benzoic acid; alpha,alpha,alpha,5-Tetrafluoro-o-toluic acid; AJ-09549; AK-36005; AN-12403; AS-19099; SC-77081; AB0031411; DB-008462; ST2406247; TR-022286; 4CH-002586; MFCD00083521; F0761; FT-0620388; ST50319731; X4501; A20064; Q-9380; 5-Fluoro-2-(trifluoromethyl)benzoic acid, 98%; I01-4924; J-517499; 654-99-9 5-fluoro-2-(trifluoromethyl)benzoic acid; 2-trifluoromethyl-5-fluorobrnzoic acid; C8H4F4O2; CID688294; 5-Fluoro-2-(trifluoromethyl)benzoic acid, 98% - 1G 1g; PubChem7873; AC1LELRR; OTF-BOA-5F;

Keywords: 654-99-9,MFCD18208176,1P003N77,5-Fluoro-2-(trifluoromethyl)benzoic acid,C8H4F4O2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P003N77 98% 100mg $6.00 $4.00 In Stock USA ADD TO CART BUY NOW
1P003N77 98% 250mg $10.00 $8.00 In Stock USA ADD TO CART BUY NOW
1P003N77 98% 1g $12.00 $9.00 In Stock USA ADD TO CART BUY NOW
1P003N77 98% 5g $26.00 $20.00 In Stock USA ADD TO CART BUY NOW
1P003N77 98% 10g $51.00 $38.00 In Stock USA ADD TO CART BUY NOW
1P003N77 95% 100g $495.00 $371.00 In Stock USA ADD TO CART BUY NOW

  • 5-Fluoro-2-(trifluoromethyl)benzoic acid is a versatile compound commonly utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its trifluoromethyl group enhances the compound's stability and lipophilicity, making it particularly useful in drug discovery and development processes. Additionally, the presence of the fluorine atom in the benzene ring enables the selective modification of organic molecules, offering opportunities for functional group manipulation and the synthesis of complex molecular structures. In modern organic synthesis, 5-Fluoro-2-(trifluoromethyl)benzoic acid plays a critical role as a key intermediate in the construction of important organic scaffolds, highlighting its significance in the field of chemical research and development.

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