89634-75-3 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-5-fluorobenzotrifluoride is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it suitable for the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-chloro-5-fluorobenzotrifluoride is utilized as an intermediate for the production of agrochemicals, contributing to the development of more effective and targeted pesticides and other agricultural chemicals.
Used in Organic Synthesis:
As a versatile building block in organic synthesis, 2-chloro-5-fluorobenzotrifluoride is employed in the manufacture of a wide range of fluorinated compounds. Its reactivity allows for the creation of novel molecules with specific properties for various applications in research and industry.
Used in Fine Chemicals Production:
2-Chloro-5-fluorobenzotrifluoride is also used in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors. Its role in this context is to provide a starting material for the synthesis of high-value specialty chemicals.
Safety Considerations:
Due to its potential to cause irritation and its flammable nature, 2-chloro-5-fluorobenzotrifluoride must be handled with caution. Proper safety protocols, including the use of personal protective equipment and adherence to storage and handling guidelines, are essential to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 89634-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,3 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89634-75:
(7*8)+(6*9)+(5*6)+(4*3)+(3*4)+(2*7)+(1*5)=183
183 % 10 = 3
So 89634-75-3 is a valid CAS Registry Number.
89634-75-3Relevant academic research and scientific papers
A Novel, Base-induced Fragmentation of Hantzsch-type 4-Aryl-1,4-dihydropyridines
McInally, Thomas,Tinker, Alan C.
, p. 1837 - 1844 (2007/10/02)
Hantzsch-type 1,4-dihydropyridine derivatives substituted with highly electron-deficient aryl groups in the 4-position, on treatment with a variety of basic reagents in non-hydroxylic solvents, undergo an unexpected and ready scission of the inter-ring bond to give the corresponding 4-unsubstituted pyridine and an arene derived from the original 4-substituent.The scope of the reaction has been investigated and possible mechanisms are discussed.
Antihypertensive 2-phenyl Hantzsch dihydropyridines
-
, (2008/06/13)
There are described compounds of formula I, STR1 in which R1 represents benzofurazanyl, pyridyl or phenyl, the pyridyl or phenyl being substituted by one or more of the groups halogen, nitro, --CN, --OR9, --S(O)p R9/
