51332-24-2 Usage
Uses
Used in Pharmaceutical Industry:
4-Bromo-N,N-dimethyl-3-(trifluoromethyl)aniline is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its presence in the molecular structure can enhance the pharmacological properties of the final product, such as potency, selectivity, and bioavailability.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Bromo-N,N-dimethyl-3-(trifluoromethyl)aniline is utilized as an intermediate in the production of agrochemicals, including pesticides and herbicides. Its unique structure allows for the creation of compounds that can effectively control pests and weeds while ensuring safety for the environment and human health.
Used in Organic Synthesis:
4-Bromo-N,N-dimethyl-3-(trifluoromethyl)aniline is used as a reagent in organic synthesis due to its unique properties and reactivity. It serves as a key component in the preparation of various organic compounds, contributing to the advancement of chemical research and the development of novel materials.
Used in Industrial Processes:
4-BROMO-N,N-DIMETHYL-3-(TRIFLUOROMETHYL)ANILINE is also used in various industrial processes, where its trifluoromethyl substituent makes it an important building block for the production of fluorinated compounds. These fluorinated compounds are of interest in drug design and optimization for a range of therapeutic indications, highlighting the compound's versatility and importance in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 51332-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,3 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51332-24:
(7*5)+(6*1)+(5*3)+(4*3)+(3*2)+(2*2)+(1*4)=82
82 % 10 = 2
So 51332-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrF3N/c1-14(2)8-4-3-6(10)5-7(8)9(11,12)13/h3-5H,1-2H3
51332-24-2Relevant academic research and scientific papers
Synthesis of Halogenated Anilines by Treatment of N, N-Dialkylaniline N-Oxides with Thionyl Halides
Reed, Hayley,Paul, Tyler R.,Chain, William J.
, p. 11359 - 11368 (2018/08/06)
The special reactivity of N,N-dialkylaniline N-oxides allows practical and convenient access to electron-rich aryl halides. A complementary pair of reaction protocols allow for the selective para-bromination or ortho-chlorination of N,N-dialkylanilines in up to 69% isolated yield. The generation of a diverse array of halogenated anilines is made possible by a temporary oxidation level increase of N,N-dialkylanilines to the corresponding N,N-dialkylaniline N-oxides and the excision of the resultant weak N-O bond via treatment with thionyl bromide or thionyl chloride at low temperature.
Low-valent niobium-mediated synthesis of indenes: Intramolecular coupling reaction of CF3 group with alkene C-H bond
Fuchibe, Kohei,Mitomi, Ken,Akiyama, Takahiko
, p. 24 - 25 (2007/10/03)
CF3 group of o-alkenyl-α,α,α-trifluorotoluenes underwent intramolecular coupling reaction with the alkene C-H bond under NbCl5/LiAlH4 system. Substituted indenes were obtained in good yields. Copyright
