219865-79-9 Usage
Description
2-METHYL-6-[(2,2,2-TRIFLUOROACETYL)AMINO]BENZOIC ACID is a chemical compound with the molecular formula C10H9F3NO3. It is a derivative of benzoic acid with a trifluoroacetyl group and an amino group attached to the 6th position of the benzene ring. 2-METHYL-6-[(2,2,2-TRIFLUOROACETYL)AMINO]BENZOIC ACID is often used as a building block in organic synthesis and medicinal chemistry due to its unique structure and functional groups, making it valuable for the development of pharmaceuticals, agrochemicals, and other specialty chemicals. Additionally, it serves as a research chemical in various scientific studies.
Uses
Used in Pharmaceutical Industry:
2-METHYL-6-[(2,2,2-TRIFLUOROACETYL)AMINO]BENZOIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its potential therapeutic properties. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 2-METHYL-6-[(2,2,2-TRIFLUOROACETYL)AMINO]BENZOIC ACID is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its specific functional groups contribute to the effectiveness of these products in controlling pests and unwanted plant growth.
Used in Organic Synthesis:
2-METHYL-6-[(2,2,2-TRIFLUOROACETYL)AMINO]BENZOIC ACID is used as a building block in organic synthesis for the creation of complex organic molecules. Its trifluoroacetyl and amino groups provide opportunities for further chemical reactions, enabling the synthesis of a wide range of specialty chemicals.
Used in Research and Development:
As a research chemical, 2-METHYL-6-[(2,2,2-TRIFLUOROACETYL)AMINO]BENZOIC ACID is employed in various scientific studies to explore its properties and potential applications. Researchers use this compound to investigate its reactivity, stability, and interactions with other molecules, contributing to the advancement of chemical knowledge and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 219865-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,8,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 219865-79:
(8*2)+(7*1)+(6*9)+(5*8)+(4*6)+(3*5)+(2*7)+(1*9)=179
179 % 10 = 9
So 219865-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H8F3NO3/c1-5-3-2-4-6(7(5)8(15)16)14-9(17)10(11,12)13/h2-4H,1H3,(H,14,17)(H,15,16)
219865-79-9Relevant articles and documents
The design and synthesis of novel orally active inhibitors of AP-1 and NF-κB mediated transcriptional activation. SAR of in vitro and in vivo studies
Palanki, Moorthy S. S.,Erdman, Paul E.,Ren, Minghuan,Suto, Mark,Bennett, Brydon L.,Manning, Anthony,Ransone, Lynn,Spooner, Cheryl,Desai, Sonal,Ow, Arnie,Totsuka, Ryuichi,Tsao, Peter,Toriumi, Wataru
, p. 4077 - 4080 (2007/10/03)
We have developed novel orally active quinazoline analogues as inhibitors of AP-1 and NF-κB mediated transcriptional activation. Among the derivatives prepared, 1-[2-(2-thienyl)quinazolin-4-ylamino]-3-methyl-3- pyrroline-2,5-dione (10) showed significant activity in an adjuvant-induced arthritis rat model by reducing the swelling by 65% in the non-injected foot. The synthesis, structure-activity relationship, and in vivo activity are described.
Xi:Irritant;
