225656-59-7 Usage
Uses
Used in Pharmaceutical Industry:
2-NITRO-4-(TRIFLUOROMETHYL)BENZYL CHLORIDE is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules with specific therapeutic properties, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 2-NITRO-4-(TRIFLUOROMETHYL)BENZYL CHLORIDE is utilized as a precursor in the synthesis of agrochemicals. Its reactive nature enables the production of compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals, helping to improve crop protection and yield.
Used in Dye and Pigment Production:
2-NITRO-4-(TRIFLUOROMETHYL)BENZYL CHLORIDE is employed as a key intermediate in the manufacturing process of dyes and pigments. Its chemical properties facilitate the synthesis of a wide range of colorants used in various industries, such as textiles, plastics, and printing inks, enhancing the colorfastness and vibrancy of the final products.
Used in Chemical Research:
2-NITRO-4-(TRIFLUOROMETHYL)BENZYL CHLORIDE also serves as a valuable compound in chemical research and development. Its unique structure and reactivity make it an interesting subject for studies aimed at understanding reaction mechanisms, exploring new synthetic routes, and discovering novel applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 225656-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,6,5 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 225656-59:
(8*2)+(7*2)+(6*5)+(5*6)+(4*5)+(3*6)+(2*5)+(1*9)=147
147 % 10 = 7
So 225656-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClF3NO2/c9-4-5-1-2-6(8(10,11)12)3-7(5)13(14)15/h1-3H,4H2
225656-59-7Relevant academic research and scientific papers
Vicarious Nucleophilic Chloromethylation of Nitroaromatics
Khutorianskyi, Viktor V.,Klepetá?ová, Blanka,Beier
supporting information, p. 5443 - 5446 (2019/07/03)
Nitroaromatics substituted with electron-acceptor or electron-donor groups undergo vicarious nucleophilic substitution with the lithium salt of dichloromethane to provide chloromethyl-substituted nitroaromatics in good to high yields. The methodology represents a new strategy for the synthesis of benzyl chlorides.
Enantioselective synthesis of diarylcyclopropanecarboaldehydes by organocatalysis
Chen, Xuyun,Yu, Yang,Liao, Ziyang,Li, Hao,Wang, Wei
supporting information, p. 5742 - 5745 (2016/12/03)
An efficient synthetic method for chiral trisubstituted diarylcyclopropanecarboaldehydes has been developed from substituted benzyl chloride and α,β-unsaturated aldehydes. The reactions were catalyzed by chiral amine catalyst under mild condition to afford the chiral diarylcyclopropanecarboaldehydes in good to high yields and up to excellent enantioselectivities.
