133932-40-8 Usage
Uses
Used in Organic Synthesis:
(1,1-difluoro-2-iodoethyl)-Benzene serves as a key intermediate in organic synthesis, where it is utilized to construct more complex organic molecules. Its unique reactivity, stemming from the presence of fluorine and iodine atoms, allows for versatile chemical transformations, making it a valuable building block in the synthesis of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (1,1-difluoro-2-iodoethyl)-Benzene is employed as a building block for the production of various drugs. Its unique chemical properties enable the development of new pharmaceuticals with improved efficacy and selectivity. (1,1-difluoro-2-iodoethyl)Benzene's reactivity allows for the creation of novel drug candidates with potential applications in treating a variety of diseases and medical conditions.
Used in Agrochemical Development:
(1,1-difluoro-2-iodoethyl)-Benzene also finds application in the agrochemical sector, where it is used as a starting material for the synthesis of new pesticides, herbicides, and other crop protection agents. Its unique properties contribute to the development of more effective and environmentally friendly agrochemicals, enhancing crop yield and quality while minimizing the impact on the environment.
Used in Material Science:
(1,1-difluoro-2-iodoethyl)Benzene's potential applications extend to the field of material science, where it is used in the development of new materials with specific properties. The presence of fluorine and iodine atoms in (1,1-difluoro-2-iodoethyl)-Benzene imparts unique characteristics to the materials, making them suitable for various applications, such as in electronics, coatings, and advanced materials.
Used in Chemical Research and Development:
(1,1-difluoro-2-iodoethyl)-Benzene is also utilized in chemical research and development, where it serves as a model compound for studying various chemical reactions and mechanisms. Its unique reactivity and properties provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge and innovation.
However, it is crucial to handle (1,1-difluoro-2-iodoethyl)-Benzene with care, as it may have potential health and environmental implications due to its chemical properties. Proper safety measures and disposal methods should be employed to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 133932-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,3 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133932-40:
(8*1)+(7*3)+(6*3)+(5*9)+(4*3)+(3*2)+(2*4)+(1*0)=118
118 % 10 = 8
So 133932-40-8 is a valid CAS Registry Number.
133932-40-8Relevant academic research and scientific papers
Conversion of the Carbonyl Group to CF2 Using IF
Rozen, Shlomo,Zamir, Dov
, p. 4695 - 4700 (2007/10/02)
A novel method for the transformation of CO -> CF2 is described.The easily made hydrazone derivatives of the carbonyl moiety are reacted under mild conditions with IF prepared directly from the corresponding elements.Various hydrazones have been examined and compared with each other.Unsubstituted ones are usually the most suitable although they are not always easy to purify and store.N-Methyl- and N,N-dimethylhydrazones also give quite satisfactory results.The more easily made dinitrophenyl hydrazones (DNPs), semicarbazones, and tosylhydrazones also react, but the yields of the desired CF2 compounds are usually lower.Oximes could also be successfully reacted.The two main byproducts of the reaction are the parent carbonyl compounds, which can be recycled, and the α-iododifluoro derivatives.The latter upon treatment with LiAlH4 or Bu3SnH were reduced to the desired product, thus increasing the overall yields.
