75039-60-0 Usage
Description
5-(DIMETHYLAMINOMETHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE, also known as a β-dimethyl amino acrylate, is an organic compound with a unique structure that features a dimethylamino group attached to a methylene bridge within a 1,3-dioxane ring. Its synthesis has been documented, and it holds potential for various applications due to its chemical properties.
Uses
Used in Chemical Synthesis:
5-(DIMETHYLAMINOMETHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable building block for the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(DIMETHYLAMINOMETHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE is used as a precursor for the development of new drugs. Its β-dimethyl amino acrylate structure can be incorporated into drug molecules to enhance their pharmacological properties, such as improving solubility, bioavailability, or targeting specific biological pathways.
Used in Material Science:
5-(DIMETHYLAMINOMETHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE is also utilized in material science for the development of novel polymers and materials with specific properties. Its ability to form covalent bonds with other molecules can contribute to the creation of materials with tailored characteristics, such as improved mechanical strength, thermal stability, or responsiveness to environmental stimuli.
Used in Research and Development:
In research and development settings, 5-(DIMETHYLAMINOMETHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE serves as a versatile compound for exploring new chemical reactions and mechanisms. Its reactivity and structural features make it an interesting subject for academic and industrial research, potentially leading to the discovery of new applications and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 75039-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,3 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75039-60:
(7*7)+(6*5)+(5*0)+(4*3)+(3*9)+(2*6)+(1*0)=130
130 % 10 = 0
So 75039-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO4/c1-9(2)13-7(11)6(5-10(3)4)8(12)14-9/h5H,1-4H3
75039-60-0Relevant articles and documents
Lactam and Amide Acetals. 52. Reaction of Dimethylformamide Diethylacetal with 2,2-Dimethyl-4,6-dioxo-1,3-dioxane (Meldrum's Acid)
Stezhko, T. V.,Solov'eva, N. P.,Kuleshova, E. F.,Granik, V. G.
, p. 151 - 153 (1988)
Depending on the conditions of carrying out the reaction of dimethylformamide diethylacetal with the Meldrum's acid, either 2,2-dimethyl-4,6-dioxo-5-(N,N-dimethylaminomethylene)-1,3-dioxane or N,N,N',N'-tetramethylformamidinium salt of 2,2-dimethyl-4,6-dioxo-5-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)methylene-1,3-dioxane are formed.The two compounds can reacts with primary amines to form N-substituted 2,2-dimethyl-4,6-dioxo-5-aminomethylene-1,3-dioxanes.
Synthesis of the microbial elicitor syringolide 2 multiply labelled with deuterium
Henschke, Julian P.,Rickards, Rodney W.
, p. 211 - 220 (2007/10/03)
Multiply-deuterated syringolide 2 3 was prepared from D-xylulose and 8- bromooctanoic acid by a convergent route based on our previously reported biomimetic synthesis of this microbial elicitor. Key steps were the thermal acylation of the anisylidene-prot
Proton Magnetic Resonance Studies of International Rotation, 10. Conformation and Stereodynamics of Dipolar Cyclic Enamines and Hydrazones
Koelle, Ulrich,Kolb, Bernd,Mannschreck, Albrecht
, p. 2545 - 2565 (2007/10/02)
2-Aminomethylene and 2-hydrazono derivatives 1-6 of carbocyclic and heterocyclic 1,3-dicarbonyl compounds which may form up to four rotational diastereoisomers were investigated by 1H and 13C NMR spectroscopy.The isomeric composition
