401-99-0 Usage
Description
3,5-Dinitrobenzotrifluoride is a light yellow crystalline powder that serves as a versatile building block in the synthesis of nitro-containing compounds. Its chemical structure and properties make it a valuable intermediate for various chemical reactions and applications.
Uses
Used in Pharmaceutical Industry:
3,5-Dinitrobenzotrifluoride is used as a synthetic intermediate for the preparation of pharmaceutical compounds. One such example is its use in the synthesis of 4-Methyl-1-[3-nitro-5-(trifluoromethyl)phenyl]-1H-imidazole (M323715), which is a compound with potential applications in the development of new drugs.
Used in Chemical Synthesis:
3,5-Dinitrobenzotrifluoride is used as a key building block in the synthesis of various nitro-containing organic compounds. Its unique structure allows for a wide range of chemical reactions, making it a valuable asset in the field of organic chemistry.
Used in Research and Development:
Due to its reactivity and structural properties, 3,5-Dinitrobenzotrifluoride is also utilized in research and development for the creation of new compounds and materials. It can be employed in the design and synthesis of novel molecules with specific properties, such as improved stability, reactivity, or biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 401-99-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 401-99:
(5*4)+(4*0)+(3*1)+(2*9)+(1*9)=50
50 % 10 = 0
So 401-99-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H3F3N2O4/c8-7(9,10)5-2-1-4(11(13)14)3-6(5)12(15)16/h1-3H
401-99-0Relevant articles and documents
Nucleophilic Substitution of Nitro Group in 3,5-Dinitrobenzotrifluoride
Khalfina,Rogozhnikova,Vlasov
, p. 1325 - 1331 (2007/10/03)
In the reaction of 3,5-dinitrobenzotrifluoride with phenols and thiophenol in the presence of potassium carbonate, fluoride- and nitrite-ions in DMF at 25-145°C, substitution of a nitro group takes place with formation of the corresponding 3-nitro-5-R-benzotrifluorides.
The Direct Trifluoromethylation of Aryl Chlorides using Burton's Reagent
Clark, James H.,McClinton, Martin A.,Blade, Robert J.
, p. 638 - 639 (2007/10/02)
The copper-dibromodifluoromethane-N,N-dimethylacetamide reaction system trifluoromethylates electronically activated aryl chlorides possessing ortho groups capable of interacting with the metal.
