2949-42-0 Usage
Uses
Used in Semiconductor Production:
Tetraisopropyltin is used as a chemical compound for the production of semiconductors. Its ability to form thin layers of tin oxide is crucial in enhancing the performance of these semiconductors.
Used in Electronic Device Manufacturing:
Tetraisopropyltin is used as a material in the manufacturing of electronic devices. Its reactivity and volatility allow for the formation of thin tin oxide layers, which are essential for the high performance of these devices.
Safety Precautions:
Despite its usefulness in production processes, Tetraisopropyltin must be handled with care due to its potential hazards upon ingestion, inhalation, or skin contact. Proper safety measures should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 2949-42-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2949-42:
(6*2)+(5*9)+(4*4)+(3*9)+(2*4)+(1*2)=110
110 % 10 = 0
So 2949-42-0 is a valid CAS Registry Number.
InChI:InChI=1/4C3H7.Sn/c4*1-3-2;/h4*3H,1-2H3;/rC12H28Sn/c1-9(2)13(10(3)4,11(5)6)12(7)8/h9-12H,1-8H3
2949-42-0Relevant academic research and scientific papers
REACTIONS OF STANNYL CATIONS
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Page/Page column 16; 17, (2018/01/17)
The present invention relates to a method of reducing, cleaving and/or coupling at least one C=O, C-O, C=C or C=N bond of a compound, using a reagent comprising a stannyl cation.
cis- and trans-(4-alkylcyclohexyl)stannanes. Isomers for stereochemical studies of substitution at saturated carbon-tin bonds
Olszowy, Henry A.,Kitching, William
, p. 1670 - 1675 (2008/10/08)
The synthesis and characterization of pure cis- and trans-(4-methylcyclohexyl)- and cis- and trans-(4-tert-butylcyclohexyl)triphenylstannanes are described. Their conversion, by hydrochloric acid induced dephenylation-isopropylation, to the corresponding triisopropylstannanes proceeds smoothly to provide stereoisomers capable of providing significant information with respect to brominolysis and trifluoroacetolysis of the carbon-tin bond.
