620627-47-6 Usage
Description
(R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide is a complex heterocyclic chemical compound with the molecular formula C16H19NO3S2. It is a derivative of oxathiazolidine, characterized by the presence of oxygen, nitrogen, and sulfur atoms in its ring structure. (R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide is known for its potential applications in various fields due to its unique structure and reactivity.
Uses
Used in Organic Synthesis:
(R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide is used as a chiral auxiliary in asymmetric synthesis for the creation of enantiomerically pure compounds. Its ability to induce chirality in the synthesized products makes it a valuable tool in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide is used as a versatile building block for the preparation of various drugs. Its unique structure allows for the development of new pharmaceuticals with potential applications in treating different medical conditions.
Used in Agrochemicals:
(R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide is also utilized as a key intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness and selectivity, contributing to improved agricultural practices.
Used in Chemical Industry:
(R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide is used as an important intermediate in the chemical industry for the production of diverse organic compounds. Its unique reactivity and structural features make it a valuable component in the synthesis of various specialty chemicals.
Used in Antibacterial Applications:
(R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide has been studied for its potential antibacterial properties, making it a candidate for development as a new class of antibacterial agents to combat resistant bacterial strains.
Used in Antifungal Applications:
Similarly, the compound has shown potential antifungal activities, which could lead to its use in the development of new antifungal drugs to treat various fungal infections.
Used in Anti-inflammatory Applications:
(R)-5,5-DiMethyl-4-phenyl-3-(toluene-4-sulfonyl)-[1,2,3]oxathiazolidine 2-oxide's potential anti-inflammatory properties make it a candidate for the development of new anti-inflammatory medications, which could be used to treat a range of inflammatory conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 620627-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,6,2 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 620627-47:
(8*6)+(7*2)+(6*0)+(5*6)+(4*2)+(3*7)+(2*4)+(1*7)=136
136 % 10 = 6
So 620627-47-6 is a valid CAS Registry Number.
620627-47-6Relevant articles and documents
Enantioselective synthesis of diverse sulfinamides and sulfinylferrocenes from phenylglycine-derived chiral sulfinyl transfer agent
Han, Zhengxu S.,Meyer, Angelica M.,Xu, Yibo,Zhang, Yongda,Busch, Robert,Shen, Sherry,Grinberg, Nelu,Lu, Bruce Z.,Krishnamurthy, Dhileep,Senanayake, Chris H.
, p. 5480 - 5484 (2011/08/09)
A new chiral sulfinyl transfer auxiliary derived from readily available phenylglycine was developed. This auxiliary is utilized to synthesize a diverse array of alkyl- and arylsulfinamides and sulfinylferrocenes in high yields and excellent ee's. The desired products are produced in a one-pot sequence from the oxathiazolidine 2-oxide by two sequential nucleophilic additions that proceed in a stereospecific manner.
