64185-12-2 Usage
Uses
Used in Organic Synthesis:
1-Tributylstannyl-3,3,3-trifluoro-1-propyne is used as a reagent for various organic synthesis processes. Its unique structure, which includes a fluorinated propyne group and a tributylstannyl group, allows it to participate in several organometallic reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Research and Development:
In the field of chemical research, 1-Tributylstannyl-3,3,3-trifluoro-1-propyne is used as a model compound to study the properties and reactivity of triorganotin compounds. This helps in understanding the behavior of organometallic compounds and their potential applications in various chemical processes.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the compound's potential use in the pharmaceutical industry could be explored due to its organometallic nature. It may be employed in the synthesis of new drug molecules or as a catalyst in pharmaceutical reactions, contributing to the development of novel therapeutic agents.
Used in Material Science:
1-Tributylstannyl-3,3,3-trifluoro-1-propyne may also find applications in material science, particularly in the development of new materials with unique properties. Its organometallic nature could be utilized in the synthesis of advanced materials, such as polymers, coatings, or composites, with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 64185-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,8 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64185-12:
(7*6)+(6*4)+(5*1)+(4*8)+(3*5)+(2*1)+(1*2)=122
122 % 10 = 2
So 64185-12-2 is a valid CAS Registry Number.
InChI:InChI=1/3C4H9.C3F3.Sn/c3*1-3-4-2;1-2-3(4,5)6;/h3*1,3-4H2,2H3;;/rC15H27F3Sn/c1-4-7-11-19(12-8-5-2,13-9-6-3)14-10-15(16,17)18/h4-9,11-13H2,1-3H3
64185-12-2Relevant academic research and scientific papers
Preparation and Functionalization of a Range of Main-Group Trifluoropropynyl Organometallic Compounds: The Application of Metalloid-Directed Carbolithiation to the Selective Synthesis of Novel Fluorocarbon Fragments
Brisdon, Alan K.,Crossley, Ian R.,Pritchard, Robin G.,Sadiq, Ghazala,Warren, John E.
, p. 5534 - 5542 (2008/10/09)
The reaction of 1,1,1,3,3-pentafluoropropane (CF3CH 2CF2H, HFC-245fa) with 3 equiv of n-butyllithium at -10 °C leads to the generation of trifluoropropynyllithium in excellent yields. This reagent reacts readily with a range of group 14 electrophiles R 4-n-EXn (R = Ph, Et; E = C, Si, Ge, Sn, Pb; X = Cl, Br) to yield the organometalloid trifluoropropynyl compounds R 4-nE(C≡CCF3)n. Three of these compounds, Ph3EC≡CCF3 (E = C, Si, Ge), have been crystallographically characterized, representing the first such study of these materials. The silane Ph3SiC≡CCF3 has been derivatized by reaction with LiAlH4 and a range of organolithium reagents (RLi, R = n-Bu, Ph, t-Bu) to afford a new series of β-CF 3-substituted vinylsilanes of the type Ph3SiCH=C(CF 3)R, with predominantly E geometry at the double bond. In the cases R = n-Bu, t-Bu, and Ph, these materials have been crystallographically characterized. Additionally, a remarkably facile cyclization pathway for Ph 3Si≡CCF3, initiated by t-BuLi, that yields the respective gem-difluorocyclopropene has been explored and is described in detail, along with its extension to a number of other systems.
