58379-84-3 Usage
Uses
Used in Polymer and Rubber Industry:
Benzene, 1-[(1-isocyano-2-methylpropyl)sulfonyl]-4-methylis used as a curing agent for improving the properties of various polymers and rubbers. Its application reason is its ability to promote the crosslinking of polymers, which results in enhanced strength, elasticity, and resistance to heat and chemicals.
Used in Chemical Synthesis:
Benzene, 1-[(1-isocyano-2-methylpropyl)sulfonyl]-4-methylcan also be used as an intermediate in the synthesis of other chemical compounds, particularly in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique chemical structure allows for further reactions and modifications to create a variety of useful compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 58379-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,7 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58379-84:
(7*5)+(6*8)+(5*3)+(4*7)+(3*9)+(2*8)+(1*4)=173
173 % 10 = 3
So 58379-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO2S/c1-9(2)12(13-4)16(14,15)11-7-5-10(3)6-8-11/h5-9,12H,1-3H3
58379-84-3Relevant academic research and scientific papers
One-pot Van Leusen synthesis of 4,5-disubstituted oxazoles in ionic liquids
Wu, Bo,Wen, Jun,Zhang, Ji,Li, Jing,Xiang, Yong-Zhe,Yu, Xiao-Qi
experimental part, p. 500 - 504 (2009/08/07)
An efficient and mild protocol for the preparation of 4,5-disubstituted oxazoles through an improved one-pot van Leusen oxazole synthesis in ionic liquids is described. The oxazole products were prepared from tosylmethyl isocyanide (TosMIC), aliphatic hal
An efficient method for the synthesis of substituted TosMIC precursors
Sisko, Joseph,Mellinger, Mark,Sheldrake, Peter W.,Baine, Neil H.
, p. 8113 - 8116 (2007/10/03)
Substituted tosylmethyl isocyanides (TosMICs) are useful reagents for which no general method of preparation is available. We describe here a high-yielding method for the synthesis of substituted tosylmethyl formamides, which are readily converted to the corresponding isocyanides.
