16898-52-5 Usage
Description
1,3-Bis(4-piperidyl)propane, also known as 4,4'-Trimethylenedipiperidine, is an organic compound that serves as a key monomer in the synthesis of various polymers and frameworks. It possesses a unique structure with two piperidine rings connected by a trimethylene bridge, which allows for versatile chemical reactions and applications.
Uses
Used in Polymer Synthesis:
1,3-Bis(4-piperidyl)propane is used as a monomer in the synthesis of hyperbranched copolymers from commercially available monomers such as divinylsulfone, 4,4'-trimethylenedipiperidine, and N-ethylenediamine. These copolymers have potential applications in various fields due to their unique properties, such as high molecular weight, low polydispersity, and tunable functionalities.
Used in Cadmium-Organic Frameworks:
1,3-Bis(4-piperidyl)propane is used as a building block in the synthesis of twoand three-dimensional cadmium-organic frameworks. These frameworks have potential applications in gas storage, catalysis, and sensing due to their high porosity, tunable pore sizes, and functionalizable surfaces.
Used in Polythioamide Formation:
1,3-Bis(4-piperidyl)propane undergoes the Willgerodt-Kindler reaction, a one-pot polycondensation with dialdehydes in the presence of sulfur, to form polythioamides. These polythioamides have potential applications in various fields, such as pharmaceuticals, materials science, and chemical sensors, due to their unique properties, such as high thermal stability, good film-forming ability, and tunable chemical reactivity.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 16898-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,9 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16898-52:
(7*1)+(6*6)+(5*8)+(4*9)+(3*8)+(2*5)+(1*2)=155
155 % 10 = 5
So 16898-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H26N2/c1-3-8-14(9-4-1)12-7-13-15-10-5-2-6-11-15/h1-13H2
16898-52-5Relevant articles and documents
A novel negative-working photoimaging material based on a base-amplifying silicone resin tethering phenylsulfonylethyl groups
Inoue, Satoru,Arimitsu, Koji,Abe, Yoshimoto,Ichimura, Kunihiro
, p. 1308 - 1309 (2007)
We have developed a base-sensitive silicone resin tethering phenylsulfonylethyl units as base-amplifying groups showing high thermal stability. The resin underwent a base proliferation reaction autocatalytically to generate amino groups on its side chains, which accelerated the base-catalyzed hydrolytic condensation of residual ethoxysilyl units in its main chain. Furthermore, a film of the resin sensitized with a photobase generator provided a negative-working photoimaging material with a high sensitivity. Copyright
Preparation of esters of phosphorus acids
-
, (2008/06/13)
Esters of phosphorus acids are prepared by an improved process whereby aromatic alcohols and phosphorus halides are reacted at specified temperatures in the presence of amine catalysts thereby providing high yields of substantially pure esters and allowing preparation of selected halogen-containing mono- and di-esters of phosphorus acids wherein halogen is directly bonded to phosphorus having substantially no side reactant contamination. The phosphorus esters are useful as intermediates in the preparation of plasticizers, oil additives and functional fluids.