32341-85-8 Usage
Chemical Class
Organosulfur compounds
Appearance
Colorless to pale yellow liquid
Solubility
Soluble in water and most organic solvents
Boiling Point
High (due to high thermal stability)
Melting Point
Not specified
Density
Not specified
Viscosity
Not specified
Flash Point
Not specified
Uses
Solvent or reagent in various organic reactions
Building block for the synthesis of other organic compounds
Stabilizer in the production of polymers
Corrosion inhibitor in industrial processes
Pharmaceutical applications (synthesis of drugs and pharmaceutical intermediates)
Safety
Handle with care due to potential irritant or toxic properties
Use appropriate safety measures (gloves, goggles, etc.)
Dispose of properly according to local regulations
Storage
Store in a cool, dry, and well-ventilated area, away from heat and open flames
Stability
High thermal stability, suitable for high-temperature applications
Environmental Impact
Not specified, but proper disposal and handling are essential to minimize environmental impact
Regulatory Status
Not specified, but may be subject to various regulations depending on the region and application
Synonyms
Not specified, but may include other names or trade names used in the industry
Chemical Structure
Not provided, but it is a derivative of ethane with two ethylsulfonyl groups attached to the 1,1-positions
Purity
Not specified, but high purity is often required for specific applications
Reactivity
Not specified, but it is important to be aware of potential reactivity with other chemicals or materials in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 32341-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,4 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32341-85:
(7*3)+(6*2)+(5*3)+(4*4)+(3*1)+(2*8)+(1*5)=88
88 % 10 = 8
So 32341-85-8 is a valid CAS Registry Number.
32341-85-8Relevant articles and documents
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Oae
, p. 41,43 (1955)
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Elimination and Addition Reactions. Part 41. Nucleophilic Eliminative Fission of Cyclopropanes: the Coiled Spring Effect of Ring Strain on Nucleofugality and its Evaluation
Hughes, Simon,Griffiths, Gwerydd,Stirling, Charles J. M.
, p. 1253 - 1264 (2007/10/02)
Rates have been measured of sulphonyl-activated eliminative ring fissions of a series of six cyclopropanes in which the leaving group is stabilised by alkoxycarbonyl, cyano, or sulphonyl groups.The measurements allow assignment of ranks (nucleofugalities) to carbon leaving groups in systems in which the connection to the leaving group is strained by incorporation in a cyclopropane ring.The values obtained are compered with those obtained for a unstrained (acyclic) analogues.Rank enhancements of about 9(log) units are obtained; these enhancements suggests that free energies of activation for leaving-group expulsion are reduced by about 53 kJmol-1, or about 46 percent of these excess of enthalpy of the strained ring, notwithstanding the small degree of ring fission in the transition structure.The effect of phenyl substitution at the leaving group suggests that cleavage of the ring is very little advanced in the transition structure, although this is variable with the nature of the leaving-group stabilisation.This is the first direct determination of the effect of strain on nucleofugality.
