481075-59-6 Usage
Uses
Used in Pharmaceutical Industry:
1-BROMO-3-IODO-5-TRIFLUOROMETHYL-BENZENE is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new chemical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-BROMO-3-IODO-5-TRIFLUOROMETHYL-BENZENE is utilized as a precursor in the synthesis of agrochemicals. Its properties contribute to the creation of compounds with pesticidal or herbicidal activities.
Used in Materials Science:
1-BROMO-3-IODO-5-TRIFLUOROMETHYL-BENZENE is employed as a component in the development of new materials with specific properties. Its structural features enable the design of materials with tailored characteristics for various applications.
Used as an Intermediate in Fine Chemicals Manufacturing:
1-BROMO-3-IODO-5-TRIFLUOROMETHYL-BENZENE serves as an intermediate in the production of various fine chemicals. Its reactivity and functional groups make it suitable for further chemical transformations to yield specialized chemical products.
Overall, the diverse applications of 1-BROMO-3-IODO-5-TRIFLUOROMETHYL-BENZENE across different industries highlight its importance as a versatile chemical compound in modern organic synthesis and material development.
Check Digit Verification of cas no
The CAS Registry Mumber 481075-59-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,0,7 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 481075-59:
(8*4)+(7*8)+(6*1)+(5*0)+(4*7)+(3*5)+(2*5)+(1*9)=156
156 % 10 = 6
So 481075-59-6 is a valid CAS Registry Number.
481075-59-6Relevant academic research and scientific papers
Fluoro- or trifluoromethyl-substituted benzyl and phenethyl alcohols: Substrates for metal-mediated site-selective functionalization
Marzi, Elena,Spitaleri, Andrea,Mongin, Florence,Schlosser, Manfred
, p. 2508 - 2517 (2007/10/03)
It was possible to functionalize the three fluorobenzyl alcohols and the three 2-(fluorophenyl)ethanols by metalation and subsequent carboxylation, the prototype electrophilic trapping reaction. Triisopropylsilyl (TIPS) outperformed methoxymethyl (MOM) as an O-protective group making seven new fluorobenzoic acids accessible in 63% average yield. Moreover, the TIPS group tolerates weakly basic and acidic media and, therefore, may facilitate further structural elaboration. The unprotected alcohols reacted more sluggishly and were unable to provide two of the targeted products (acids 1 and 2). The yield averaged only 46% in the five other cases (acids 3-7). The direct metalation of fluorinated benzyl and phenethyl alcohols remains nevertheless an attractive option because of its operational simplicity. All three (trifluoromethyl)benzyl alcohols and two of the three (trifluoromethyl)phenethyl alcohol isomers were successfully submitted to the metalation/functionalization sequence. These five starting materials gave rise to a total of nine new benzoic acids or lactones (compounds 8-14 and 17-18). Despite the poor yields (31% on average), the organometallic methods employed are, in general, extremely selective, economical and easy to perform. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
