878285-13-3 Usage
Uses
Used in Pharmaceutical Industry:
3,5-Difluoro-4-methylaniline serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, making it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-Difluoro-4-methylaniline is utilized in the production of pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness in protecting crops and controlling pests, thereby contributing to increased agricultural productivity.
Used in Dye Industry:
3,5-Difluoro-4-methylaniline is also employed in the synthesis of dyes, where its chemical properties contribute to the creation of dyes with specific color characteristics and improved performance. This makes it an important substance in the textile and other industries that rely on colorants.
Used as an Intermediate in Organic Compounds Production:
Beyond its direct applications, 3,5-Difluoro-4-methylaniline is a key intermediate in the production of other organic compounds. Its role in the synthesis of these compounds highlights its importance in organic chemistry and the broader chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 878285-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,2,8 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 878285-13:
(8*8)+(7*7)+(6*8)+(5*2)+(4*8)+(3*5)+(2*1)+(1*3)=223
223 % 10 = 3
So 878285-13-3 is a valid CAS Registry Number.
878285-13-3Relevant academic research and scientific papers
Alric,Marquet,Billard,Langlois
, p. 661 - 667 (2005)
Anilines are mainly or selectively fluorinated in the meta-position with F2 when dissolved in triflic acid, sometimes in the presence of small quantities of antimony pentafluoride. The regioselectivity is increased when an electron-donating substituent is present at the para-position.
