16248-90-1 Usage
Uses
Used in Organic Synthesis:
Bis(diethyldithiocarbamic acid) tin(II) salt is used as a stabilizer for enhancing the stability of reactive intermediates in organic synthesis, thereby improving the yield and efficiency of chemical reactions.
Used in Polymerization Reactions:
In the polymer industry, Bis(diethyldithiocarbamic acid) tin(II) salt is utilized as a catalyst to facilitate and control the polymerization process, leading to the production of polymers with desired properties.
Used in Metal Ion Extraction and Separation:
Bis(diethyldithiocarbamic acid) tin(II) salt is employed as an extracting agent in the separation and purification of metal ions from aqueous solutions, thanks to its ability to form stable complexes with these ions.
Used in Pharmaceutical Research:
Bis(diethyldithiocarbamic acid) tin(II) salt is studied for its potential as an anti-cancer agent, with research showing its effectiveness in inhibiting the growth of certain types of cancer cells, thus warranting further investigation for therapeutic applications.
Used in Environmental Applications:
In environmental science, Bis(diethyldithiocarbamic acid) tin(II) salt may be used for the remediation of metal-contaminated water and soil, given its metal ion extraction capabilities.
Check Digit Verification of cas no
The CAS Registry Mumber 16248-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,4 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16248-90:
(7*1)+(6*6)+(5*2)+(4*4)+(3*8)+(2*9)+(1*0)=111
111 % 10 = 1
So 16248-90-1 is a valid CAS Registry Number.
InChI:InChI=1/2C5H11NS2.Sn/c2*1-3-6(4-2)5(7)8;/h2*3-4H2,1-2H3,(H,7,8);/q;;+2/p-2
16248-90-1Relevant academic research and scientific papers
Synthesis and thermal decomposition studies of homo- and heteroleptic tin(IV) thiolates and dithiocarbamates: Molecular precursors for tin sulfides
Barone, Giampaolo,Chaplin, Tracy,Hibbert, Thomas G.,Kana, Aliki T.,Mahon, Mary F.,Molloy, Kieran C.,Worsley, Ian D.,Parkin, Ivan P.,Price, Louise S.
, p. 1085 - 1092 (2007/10/03)
The syntheses and X-ray structures of novel heteroleptic thiolate/dithiocarbamate derivatives (Et2NCS2)2(RS)2Sn (R = Cy, CH2CF3) have been examined and their thermal decompositions compared with those of selected tinq and tin(IV) dithiocarbamates. The heteroleptic species decompose to SnS by initial elimination of RSSR to afford (Et2NCS2)2Sn and subsequent loss of [Et2NC(S)]2S. In contrast, (Et2NrS2)4Sn decomposes via [(Et2NCS2)2SnS]2, whose structure has been determined, and finally to SnS2 by sequential elimination of [Et2NC(S)]2S. The two families of compounds, (R2NCS2)4Sn and (Et2NCS2)2(RS)2Sn, thus provide single-source materials for bulk SnS2 and SnS, respectively, by virtue of their differing decomposition pathways. Preliminary CVD experiments with (Et2NCS2)2(CyS)2Sn are also reported.
