78946-84-6 Usage
Uses
Used in Medicinal Chemistry:
(11R,15R)-11,15-dimethyl-1,4,7,10-tetraoxa-13-azacyclopentadecane is used as a potential candidate in medicinal chemistry due to its unique structure and the presence of heteroatoms, which can contribute to its interaction with biological targets and its potential as a pharmaceutical agent.
Used in Material Science:
In the field of material science, (11R,15R)-11,15-dimethyl-1,4,7,10-tetraoxa-13-azacyclopentadecane may be utilized for the development of new materials with specific properties, such as improved stability or reactivity, owing to its heterocycle nature and the presence of oxygen and nitrogen atoms.
Used as a Reagent in Organic Synthesis:
(11R,15R)-11,15-dimethyl-1,4,7,10-tetraoxa-13-azacyclopentadecane can be employed as a reagent in organic synthesis, where its unique structure and functional groups can be used to facilitate specific chemical reactions or to synthesize complex organic molecules with desired properties.
Check Digit Verification of cas no
The CAS Registry Mumber 78946-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78946-84:
(7*7)+(6*8)+(5*9)+(4*4)+(3*6)+(2*8)+(1*4)=196
196 % 10 = 6
So 78946-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H25NO4/c1-11-9-13-10-12(2)17-8-6-15-4-3-14-5-7-16-11/h11-13H,3-10H2,1-2H3
78946-84-6Relevant academic research and scientific papers
Synthesis of Monoaza Crown Ethers from N,N-Diamines and Oligoethylene Glycol Di(p-toluenesulfonates) or Corresponding Dichlorides
Maeda, Hirokazu,Furuyoshi, Shigeo,Nakatsuji, Yohji,Okahara, Mitsuo
, p. 212 - 218 (2007/10/02)
Monoaza crown ethers were prepared in satisfactory yields by the one-step reaction between diethanolamine or N,N-diamines and oligoethylene glycol di(p-toluenesulfonates) or corresponding dichlorides in t-butyl alcohol/dioxane in the presence of sodium or potassium t-butoxide.The reaction conditions in the preparation of monoaza 15- and 18-crown ethers were studied.Various monoaza crown ethers having substituents were also prepared and their properties were investigated.
Facile Synthesis of Monoaza Crown Ethers
Maeda, Hirokazu,Nakatsuji, Yohji,Okahara, Mitsuo
, p. 471 - 472 (2007/10/02)
A facile one-step synthesis of monoaza crown ethers by treatment of dialkanolamines with oligoethylene glycol di(toluene-p-sulphonates) or dichlorides in ButOM-ButOH (M = Na, K) is described.
