70912-54-8 Usage
Uses
Used in Organic Synthesis:
2,2-DIMETHYL-5-(2-HEXAHYDROAZEPINYLIDENE)-1,3-DIOXAN-4,6-DIONE is used as a building block in organic synthesis for the preparation of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Chemical Research:
In the field of chemical research, 2,2-DIMETHYL-5-(2-HEXAHYDROAZEPINYLIDENE)-1,3-DIOXAN-4,6-DIONE serves as a valuable reagent. It aids scientists in understanding the properties and reactions of complex organic molecules, contributing to the advancement of chemical knowledge.
Used in Pharmaceutical Development:
2,2-DIMETHYL-5-(2-HEXAHYDROAZEPINYLIDENE)-1,3-DIOXAN-4,6-DIONE is utilized as a reagent in the development of new pharmaceuticals. Its structural features make it a promising candidate for the synthesis of novel drug molecules with potential therapeutic applications.
Used in Material Science:
In material science, 2,2-DIMETHYL-5-(2-HEXAHYDROAZEPINYLIDENE)-1,3-DIOXAN-4,6-DIONE is employed in the development of new materials. Its incorporation into various material systems can lead to the creation of innovative products with improved properties and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 70912-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,1 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70912-54:
(7*7)+(6*0)+(5*9)+(4*1)+(3*2)+(2*5)+(1*4)=118
118 % 10 = 8
So 70912-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO4/c1-12(2)16-10(14)9(11(15)17-12)8-6-4-3-5-7-13-8/h9H,3-7H2,1-2H3
70912-54-8Relevant academic research and scientific papers
Synthesis of [1,2-A]-fused tricyclic dihydroquinolines by palladiumcatalyzed intramolecular C-N cross-coupling of polarized heterocyclic enamines
Bro?, B?etislav,R??i?ková, Zdeňka,?im?nek, Petr
supporting information, p. 118 - 141 (2016/10/22)
A simple methodology for [1,2-A]-fused tricyclic dihydroquinolines is established. The key ste of the methodology is an intramolecular Buchwald-Hartwig amination reaction of suitabl halogenated (both bromo and chloro) cyclic enaminoketones, enaminoesters and enaminonitrile with various ring size (from five-to seven-membered). Optimal reaction conditions (palladiu source, base, ligand) depend on the ring size of the starting enamine, giving 65-98% yield of th tricyclic product. A treatment of the products with perchloric acid gives respective quinoliniu perchlorates.
Studies on Pyrrolidones. Synthesis and N-Alkylation of &β-Enaminoesters Derived from Pyroglutamic Acid
Fasseur, Dominique,Rigo, Benoit,Leduc, Catherine,Cauliez, Pascal,Couturier, Daniel
, p. 1285 - 1291 (2007/10/02)
The condensation of iminoether 7, derived from pyroglutamic acid (4), with active methylene reagents such as Meldrum's acid or methyl cyanoacetate, lead to β-enaminoesters 2.Solid-liquid phase transfer N-alkylation of these compounds is described.
Reaction des carbanions maloniques sur le S-methyl ε-thiocaprolactime
Lhommet, Gerard,Richaud, Marie, Genevieve,Maitte, Piere
, p. 431 - 432 (2007/10/02)
S-Methyl-ε-thiocaprolactim reacted with methylene compounds such as β-diketones, β-keto esters or some malonates.We have shown that S-methyl-ε-thiocaprolactim is a more satisfactory activated form of the amide than O-methyl-ε-caprolactim.
