Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 120013-39-0, Name is 5,6-Dimethoxy-2-(4-piperidinylmethyl)-1-indanone hydrochloride, SMILES is Cl.COC2=C(C=C1C(C(CC1=C2)CC3CCNCC3)=O)OC, in an article , author is Knight, Jonathon D., once mentioned of 120013-39-0, Formula: C17H24ClNO3.
Synthesis and radical copolymerization of novel propyl cyanoacrylate monomers
Novel phenyl-trisubstituted propyl 3-(R-phenyl)-2-cyanoacrylates (where R is 2,4,5-trimethyl, 2,4,6-trimethyl, 2,3-dimethyl-4-methoxy, 2,5-dimethyl-4-methoxy, 2,4-dimethoxy-3-methyl, 2,4-dimethoxy-6-methyl, 4-hydoxy-3,5-dimethyl, 2,3,4-trimethoxy, 2,4,5-trimethoxy, 2,4,6-trimethoxy, 3,4,5-trimethoxy) were prepared using piperidine-catalyzed condensation of substituted benzoic aldehydes and propyl ester of cyanoacetic acid with good yields (72-97 wt%). The ethenylbenzene copolymerization of cyanoacrylates (at 3/1 mol feed ratio) in solution with radical initiation at 70 degrees C resulted in formation of copolymers having M-W 3.9 to 27.8 kD and 8.4-25.8 mol% of cyanoacrylate. FTIR, H-1 and C-13 NMR were used to analyze the structure. Thermal behavior of the copolymers was analyzed by DSC, T-g (81-129 degrees C) and TGA. Decomposition of the copolymers in nitrogen occurred in two steps, first in the 200-500 degrees C range with residue (0.5-7.3 wt%)and then in the 500-800 degrees C range.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 120013-39-0, you can contact me at any time and look forward to more communication. Formula: C17H24ClNO3.
Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem