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Methanesulfonyloxyacetonitrile, also known as methanesulfonyl cyanide or mesityl oxide cyanohydrin, is an organic compound with the chemical formula C4H7NO2S. It is a colorless liquid that is soluble in water and has a pungent odor. methanesulfonyloxyacetonitrile is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is produced through the reaction of acetonitrile with methanesulfonyl chloride, and its chemical properties include reactivity towards nucleophiles due to the presence of the cyano group and the离去 ability of the methanesulfonyl group. Methanesulfonyloxyacetonitrile is also known for its use in the preparation of chiral auxiliaries and ligands in asymmetric synthesis, highlighting its importance in the field of organic chemistry.

3586-51-4

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3586-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3586-51-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3586-51:
(6*3)+(5*5)+(4*8)+(3*6)+(2*5)+(1*1)=104
104 % 10 = 4
So 3586-51-4 is a valid CAS Registry Number.

3586-51-4Relevant academic research and scientific papers

Direct Spectroscopic Detection of Sulfonyloxy Radicals and First Measurements of Their Absolute Reactivities

Korth, Hans-Gert,Neville, Anthony G.,Lusztyk, Janusz

, p. 8835 - 8839 (2007/10/02)

Two sulfonyloxyl radicals, CH3S(=O)2O., 2a, and 3-CF3C6H4S(=O)2O., 2b, have been generated by 308-nm laser flash photolysis (LFP) of their parent symmetrical peroxides in CH3CN solution, in which they have lifetimes of 7-20 μs.Both radicals exhibit a broad, structureless absorption similar to that known for SO4.- with λmax ca. 450 nm.This absorption can be bleached for 2a but not for 2b by firing a second laser at 480 nm, presumably reflecting a photoinduced cleavage of the H3C-SO3. bond.Radicals 2a and 2b react with the acetonitrile solvent by abstraction of a hydrogen atom, kH ca. 1.6*105 M-1 s-1, kH/kD ca. 2.0.Bimolecular rate constants for attack of these radicals on cyclohexane (viz., 1.9*108 and 6.5*108 M-1 s-1 for 2a and 2b, respectively) and chloroform (viz. ca., 3*105 M-1 s-1 for both) demonstrate that they are more reactive than almost all other oxygen-centered radicals.Product studies demonstrate that both the photodecomposition and the thermal decomposition of the parent peroxides yield the corresponding sulfonyloxy radicals, a result that contrasts with that we have previously obtained for the decomposition of 2, which yields radicals on photolysis but few if any radicals on thermolysis.Semiempirical AM1/PM3-UHF calculations on 2a are also reported.

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