6211-59-2 Usage
Molecular Structure
2,3-dihydrothiophene-3-ol 1,1-dioxide is a chemical compound that contains a five-membered ring with four carbon atoms and one sulfur atom.
Type of Compound
It is an organosulfur compound.
Uses
It is commonly used in the synthesis of pharmaceuticals and agrochemicals.
Chemical Reactivity
2,3-dihydrothiophene-3-ol 1,1-dioxide is known for its ability to act as a reducing agent in various chemical reactions.
Odor
It has a distinct odor.
Toxicity
It is considered to be toxic if ingested or inhaled.
Environmental Impact
2,3-dihydrothiophene-3-ol 1,1-dioxide is known for its potential environmental impact and is regulated in certain jurisdictions.
Check Digit Verification of cas no
The CAS Registry Mumber 6211-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6211-59:
(6*6)+(5*2)+(4*1)+(3*1)+(2*5)+(1*9)=72
72 % 10 = 2
So 6211-59-2 is a valid CAS Registry Number.
6211-59-2Relevant articles and documents
Merging Halogen-Atom Transfer (XAT) and Cobalt Catalysis to Override E2-Selectivity in the Elimination of Alkyl Halides: A Mild Route towardcontra-Thermodynamic Olefins
Zhao, Huaibo,McMillan, Alastair J.,Constantin, Timothée,Mykura, Rory C.,Juliá, Fabio,Leonori, Daniele
supporting information, p. 14806 - 14813 (2021/09/18)
We report here a mechanistically distinct tactic to carry E2-type eliminations on alkyl halides. This strategy exploits the interplay of α-aminoalkyl radical-mediated halogen-atom transfer (XAT) with desaturative cobalt catalysis. The methodology is high-yielding, tolerates many functionalities, and was used to access industrially relevant materials. In contrast to thermal E2 eliminations where unsymmetrical substrates give regioisomeric mixtures, this approach enables, by fine-tuning of the electronic and steric properties of the cobalt catalyst, to obtain high olefin positional selectivity. This unprecedented mechanistic feature has allowed access tocontra-thermodynamic olefins, elusive by E2 eliminations.
