93857-90-0 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-5-Fluorotoluene is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique molecular structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Chloro-5-Fluorotoluene serves as a crucial building block for the production of pesticides and other crop protection agents. Its incorporation into these products enhances their effectiveness in controlling pests and diseases, thereby improving agricultural productivity.
Used in Dye and Pigment Production:
3-Chloro-5-Fluorotoluene is utilized as an intermediate in the manufacturing process of dyes and pigments. Its presence in these compounds imparts specific color characteristics and properties, making it an essential component in the colorant industry.
Used in Organic Compound Synthesis:
As a versatile chemical intermediate, 3-Chloro-5-Fluorotoluene is employed in the synthesis of a wide range of organic compounds. Its reactivity and functional groups enable the formation of various derivatives, expanding the scope of organic chemistry and its applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 93857-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,8,5 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93857-90:
(7*9)+(6*3)+(5*8)+(4*5)+(3*7)+(2*9)+(1*0)=180
180 % 10 = 0
So 93857-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClF/c1-5-2-6(8)4-7(9)3-5/h2-4H,1H3
93857-90-0Relevant academic research and scientific papers
Benzylated 1,2,3-triazoles as anticoccidiostats
Bochis,Chabala,Harris,Peterson,Barash,Beattie,Brown,Graham,Waksmunski,Tischler,Joshua,Smith,Colwell,Wyvratt Jr.,Fisher,Tamas,Nicolich,Schleim,Wilks
, p. 2843 - 2852 (2007/10/02)
Substituted 5-amino-4-carbamoyl-1,2,3-triazoles 3a-w were prepared by two synthetic schemes and evaluated in vivo for anticoccidial activity. Both schemes proceeded by brominating appropriately substituted toluenes 4a-s,v to 5a-s,v. In Scheme I, the brominated benzyl analogues 5 were converted to the corresponding benzyl azides 6, which were treated with cyanoacetamide to yield 1-substituted-5-amino-4-carbamoyl-1,2,3-triazoles 3. In Scheme II, the benzyl halides 5 were employed to alkylate the sodium salt of 5-amino-4-carbamoyl-1,2,3-triazole (7). Preliminary screening data against Eimeria acervulina and E. tenella in chickens suggested structural requirements for maximizing activity. Further evaluation against a relatively resistant series of eight Eimeria field isolates revealed L-651,582 (3a) to be a highly effective coccidiostat. However, unacceptable tissue residues precluded further development. Mechanistic studies on this series of 5-amino-4-carbamoyl-1,2,3-triazoles and, in particular, on L-651,582 (3a) revealed that its mode of action does not involve inhibition of IMP dehydrogenase, but probably interferes with host cell calcium entry. In addition, L-651,582 has been found to have antiproliferative activity in several disease models and was recently reported to possess antimetastatic activity in a model of ovarian cancer progression.
