126541-87-5 Usage
Uses
Used in Pharmaceutical Industry:
3-Hydroxy-4-trifluoromethylbenzoic acid is used as an intermediate in the synthesis of various drugs. Its unique structure and properties contribute to the development of pharmaceuticals with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Hydroxy-4-trifluoromethylbenzoic acid serves as an intermediate for the production of agrochemical products. Its role in this industry is crucial for creating compounds that address various agricultural needs.
Used in Specialty Chemicals Production:
3-Hydroxy-4-trifluoromethylbenzoic acid is used as a building block in the creation of specialty chemicals. Its incorporation into these chemicals enhances their performance and applicability in specialized areas.
Used in Organic Compounds Synthesis:
3-Hydroxy-4-trifluoromethylbenzoic acid is also utilized in the synthesis of organic compounds, broadening its applications across different industries that rely on organic chemistry for their products.
Safety Note:
It is important to handle 3-Hydroxy-4-trifluoromethylbenzoic acid with care, as it can pose hazards if ingested, inhaled, or absorbed through the skin, emphasizing the need for proper safety measures during its use and manipulation.
Check Digit Verification of cas no
The CAS Registry Mumber 126541-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,4 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126541-87:
(8*1)+(7*2)+(6*6)+(5*5)+(4*4)+(3*1)+(2*8)+(1*7)=125
125 % 10 = 5
So 126541-87-5 is a valid CAS Registry Number.
126541-87-5Relevant articles and documents
Demethyl(trifluoromethyl)actinomycins
Giencke, Astrid,Lackner, Helmut
, p. 569 - 579 (2007/10/02)
The synthesis of new 4-(trifluoromethyl)benzoic acid derivatives 2-10 and their coupling with amino acids and peptides 12, 13, 15 is described.They serve as precursors for the synthesis of the hitherto unknown demethyl(trifluoromethyl)actinocin dimethyl esters 11, demethyl-trifluoromethyl-actinocinyl peptides 14, 16, 18 and the demethyl-trifluoromethyl-actinomycins 17.Although spacially comparable with the methyl residues, the 4- and 6-trifluoromethyl groups have unexpected strong influences on the antibiotic and cytostatic properties of the actinomycins.The CH3/CF3 exchange makes it possible to bring NMR-analytically useful hetero nuclei into the centre of the actinomycin/DNA complex (Figure 1).
