54953-79-6 Usage
Uses
Used in Pharmaceutical Industry:
5,5-DIMETHYL-[1,3]OXAZINAN-2-ONE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a building block for the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agricultural Chemical Industry:
In the agricultural sector, 5,5-DIMETHYL-[1,3]OXAZINAN-2-ONE serves as an intermediate for the production of agricultural chemicals. Its role in creating effective compounds for pest control and crop protection underscores its importance in this industry.
Used in Polymer and Material Science:
5,5-DIMETHYL-[1,3]OXAZINAN-2-ONE is utilized in the manufacturing of polymers and materials. Its chemical properties make it a valuable component in developing new materials with specific characteristics for various applications, including coatings, adhesives, and composites.
Used in Research for Biological Activities:
5,5-DIMETHYL-[1,3]OXAZINAN-2-ONE is studied for its potential biological activities, such as antibacterial and antifungal properties. This research is crucial for discovering new agents that can combat resistant strains of bacteria and fungi, contributing to the field of antimicrobial therapy.
The diverse applications of 5,5-DIMETHYL-[1,3]OXAZINAN-2-ONE reflect its versatility and the ongoing exploration of its uses in research and industrial settings. Its presence across different sectors highlights the compound's significance in modern scientific and technological advancements.
Check Digit Verification of cas no
The CAS Registry Mumber 54953-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,5 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54953-79:
(7*5)+(6*4)+(5*9)+(4*5)+(3*3)+(2*7)+(1*9)=156
156 % 10 = 6
So 54953-79-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c1-6(2)3-7-5(8)9-4-6/h3-4H2,1-2H3,(H,7,8)
54953-79-6Relevant academic research and scientific papers
Carbon dioxide as a carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas: Scope and limitations
Paz, Jairo,Perez-Balado, Carlos,Iglesias, Beatriz,Munoz, Luis
supporting information; experimental part, p. 3037 - 3046 (2010/07/15)
Carbon dioxide can be used as a convenient carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas. The transient carbamate anion generated by treating a primary or secondary amine group in basic media can be activated with phosphorylating agents such as Diphenylphosphoryl azide (DPPA) and Diphenyl chlorophosphate (DPPCl) but also with other types of electrophiles such as SOCl2, TsCl, or AcCl. The intramolecular trapping of the activated carbamate by a hydroxyl group leads to the formation of 2-oxazolidinones or 2-oxazinones in good to excellent yields. This methodology was successfully applied to the synthesis of cyclic ureas up to 7-membered rings from the corresponding diamines.
Selective catalytic oxidative carbonylation of amino alcohols to ureas
Diaz, Delmy J.,Hylton, Keisha-Gay,McElwee-White, Lisa
, p. 734 - 738 (2007/10/03)
Amino alcohols undergo W(CO)6-catalyzed oxidative carbonylation to the corresponding hydroxyalkylureas without protection of the hydroxyl group. Selected examples of 1,2-, 1,3-, 1,4-, and 1,5-amino alcohols were converted to the ureas in good to excellent yields, with only small amounts of the cyclic carbamates being formed. In contrast, the phosgene derivatives CDI and DMDTC undergo stoichiometric reactions with the amino alcohol substrates to afford ureas and cyclic carbamates with variable selectivity.
