180134-15-0 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Methoxy-4,6-di(trifluoromethyl)benzoic acid is utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with enhanced properties, such as improved potency, selectivity, and bioavailability.
Used in Agrochemical Production:
In the agrochemical industry, 2-Methoxy-4,6-di(trifluoromethyl)benzoic acid serves as an essential component in the production of various agrochemicals. Its incorporation into these compounds can lead to more effective and targeted pest control solutions.
Used in Organic Synthesis as a Building Block:
2-Methoxy-4,6-di(trifluoromethyl)benzoic acid is employed as a building block in organic synthesis, enabling the creation of a wide range of organic compounds with diverse applications. Its unique functional groups facilitate various chemical reactions, expanding the scope of synthetic chemistry.
Used in Dye and Pigment Production:
As an intermediate in the production of dyes and pigments, 2-Methoxy-4,6-di(trifluoromethyl)benzoic acid contributes to the development of novel colorants with improved properties, such as increased stability, brightness, and colorfastness. Its presence in these compounds can lead to innovative applications in various industries, including textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 180134-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,1,3 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 180134-15:
(8*1)+(7*8)+(6*0)+(5*1)+(4*3)+(3*4)+(2*1)+(1*5)=100
100 % 10 = 0
So 180134-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H6F6O3/c1-19-6-3-4(9(11,12)13)2-5(10(14,15)16)7(6)8(17)18/h2-3H,1H3,(H,17,18)
180134-15-0Relevant articles and documents
2-Methoxy-4,6-bis(trifluoromethyl)phenyllithium: A new stable aryllithium useful as an intermediate to bis(trifluoromethyl)aromatics
Dmowski, Wojciech,Piasecka-Maciejewska, Krystyna
, p. 59 - 63 (2007/10/03)
A method for the preparation of 3,5-bis(trifluoromethyl)anisole (3) has been developed. Lithiation of 3 occurred exclusively at the position ortho to the CH3O group to give a thermally stable lithium derivative 6 which readily undergoes conventional reactions with a number of electrophiles. Formylation and carboxylation of 6 gave bis(trifluoromethyl) derivatives of salicylic aldehyde and salicylic acid 9-12 in good yields.
