Category: 1008361-77-0

《Self-Assembly of a Giant Molecular Solomon Link from 30 Subcomponents》 was published in Angewandte Chemie, International Edition in 2014. These research results belong to Schouwey, Clement; Holstein, Julian J.; Scopelliti, Rosario; Zhurov, Konstantin O.; Nagornov, Konstantin O.; Tsybin, Yury O.; Smart, Oliver S.; Bricogne, Gerard; Severin, Kay. SDS of cas: 1008361-77-0 The article mentions the following:

The synthesis of topol. complex structures, such as links and knots, is one of the current challenges in supramol. chem. The so-called Solomon link consists of two doubly interlocked rings. Despite being a rather simple link from a topol. point of view, only few mol. versions of this link have been described so far. Here, the authors report the quant. synthesis of a giant mol. Solomon link from 30 subcomponents. The highly charged structure is formed by assembly of 12 cis-blocked Pt2+ complexes, six Cu+ ions, and 12 rigid N-donor ligands. Each of the two interlocked rings is composed of six repeating Pt(ligand) units, while the six Cu+ ions connect the two rings. With a mol. weight of nearly 12 kDa and a diameter of 44.2 Å, this complex is the largest non-DNA-based Solomon link described so far. Furthermore, it represents a mol. version of a “”stick link””. The experimental process involved the reaction of 3-Bromo-6-iodo-2-methylpyridine(cas: 1008361-77-0SDS of cas: 1008361-77-0)

3-Bromo-6-iodo-2-methylpyridine(cas: 1008361-77-0) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.SDS of cas: 1008361-77-0

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Recommanded Product: 3-Bromo-6-iodo-2-methylpyridineOn September 30, 2016 ,《Povarov reaction, scope and limitations: Preparation of diversely heterocyclic tetrahydro-1H-cyclopenta[c]quinolines》 was published in Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry. The article was written by Ninoa, Patricia; Cabaa, Marta; Aguilarb, Nuria; Terricabrasb, Emma; Albericioc, Fernando; Fernandez, Joan-Carles. The article contains the following contents:

Herein, parallel synthesis of diverse heterocyclic-tetrahydro-1H-cyclopenta[c]quinolines, e.g., I in excellent yields and high endo diastereoselectivity has been described. These compounds are highly functionalized natural product-like tricyclic systems, which may be useful as biol. relevant targets. Fine tuning of the reaction conditions need to be performed depending on the nature and mol. structure of the heterocyclic aromatic carbaldehyde, as well as the choice of the Lewis acid catalyst. Synthesis of the heterocyclic aromatic aldehyde precursors of the Povarov reaction is also described. The experimental part of the paper was very detailed, including the reaction process of 3-Bromo-6-iodo-2-methylpyridine(cas: 1008361-77-0Recommanded Product: 3-Bromo-6-iodo-2-methylpyridine)

3-Bromo-6-iodo-2-methylpyridine(cas: 1008361-77-0) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Recommanded Product: 3-Bromo-6-iodo-2-methylpyridine

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com