61702-08-7 Usage
Description
(3E)-N-(4-tert-butylpyridin-2-yl)-3-(4-tert-butylpyridin-2-yl)imino-isoindol-1-amine is an organic compound with the molecular formula C22H26N4. It is a synthetic compound containing two 4-tert-butylpyridin-2-yl groups attached to an iminoisoindoline core.
Used in Pharmaceutical Research and Development:
(3E)-N-(4-tert-butylpyridin-2-yl)-3-(4-tert-butylpyridin-2-yl)imino-isoindol-1-amine is used as a research compound for the development of new pharmaceuticals. Its unique structure and properties make it a promising candidate for the design and synthesis of novel drug molecules.
Used in Organic Synthesis:
(3E)-N-(4-tert-butylpyridin-2-yl)-3-(4-tert-butylpyridin-2-yl)imino-isoindol-1-amine is also used as a building block in organic synthesis. Its versatile structure allows for further functionalization and modification, enabling the synthesis of a wide range of organic compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 61702-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,0 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61702-08:
(7*6)+(6*1)+(5*7)+(4*0)+(3*2)+(2*0)+(1*8)=97
97 % 10 = 7
So 61702-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C26H29N5/c1-25(2,3)17-11-13-27-21(15-17)29-23-19-9-7-8-10-20(19)24(31-23)30-22-16-18(12-14-28-22)26(4,5)6/h7-16H,1-6H3,(H,27,28,29,30,31)
61702-08-7Relevant articles and documents
Spin Crossover and Valence Tautomerism in Neutral Homoleptic Iron Complexes of Bis(pyridylimino)isoindolines
Scheja, Anne,Baabe, Dirk,Menzel, Dirk,Pietzonka, Clemens,Schweyen, Peter,Br?ring, Martin
, p. 14196 - 14204 (2015/09/28)
Homoleptic iron complexes of six bis(pyridylimino)isoindoline (bpi) ligands with different substituents (H, Me, Et, tBu, OMe, NMe2) at the 4-positions of the pyridine moieties have been prepared and studied with regard to temperature-dependent spin and redox states by a combination of 57Fe M?ssbauer spectroscopy, SQUID magnetometry, single-crystal X-ray diffraction analysis, X-band EPR, and 1H NMR spectroscopy. While the H-, methyl-, and ethyl-substituted complexes remain in a pure high-spin state irrespective of the temperature, the 4-tert-butyl-substituted derivative shows spin-crossover behavior. The methoxy- and dimethylamino-substituted compounds were found to easily undergo oxidation. In the crystalline state, valence tautomeric behavior was observed for the methoxy derivative as a thermally activated charge-transfer transition, accompanied by a spin crossover above 200 K. The valence tautomerism leads to a chelate with one of the bpi ligands as a dianion radical L2-. and with an effective spin of S=2.
