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Two sandwiched cluster organic frameworks, Eu6(OH)2Cu9I6L12(ox)3.H2O.ClO4 (FJ-23, HL=4-pyridin- 4-yl-benzonic acid, ox=oxalate) and Eu6Cu7I7L12(OAc)6(H2O)2.2H2O (FJ-24, OAc=acetate) with bnn hexagonal BN topologies have been successfully made; these frameworks were assembled by nanosized graphene-like lanthanide wheel clusters and nanoscale trigonal prism metalloligands. The cooperation of small equatorial ligands and axially trigonal prism metalloligands plays a key role in the construction of such 5-connected nets. Furthermore, the thermal stabilities and chiral characteristics were also studied.

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Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

New Advances in Chemical Research in 2021. Chemistry is a science major with cience and engineering. The main research directions are chemical synthesis, and research on the structure and performance of functional materials.In a patent, 57196-62-0, name is 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride, introducing its new discovery. Related Products of 57196-62-0

As globalization and rapid population growth have raised global energy needs, the demand for nuclear energy has increased drastically. To make use of such energy more reliably, the efficient disposal of nuclear wastes has become a major challenge. With this in mind, numerous research efforts have been put to safely store, capture, and immobilize radioactive waste. As a result, a variety of sorbent materials with different physical, chemical, and structural properties have been invented or discovered. The maximum removal capacity of these sorbents were then assessed for a variety of radionuclides in soluble and/or gaseous forms. The pre-/post-synthetic modification of these sorbent materials has also been investigated intensively to help enhance their overall stability, tunability, and capacity without altering or damaging the main framework. In this review, we explored the performance of different materials for the sorption of most important radionuclide species including uranium, cobalt, europium, iodine, cesium, strontium, technetium, krypton, xenon, and argon. To begin with, we classified sorbent materials into three categories in light of their structural evolvement over time. We also described the critical factors to consider for the proper application of these categorized sorbents (e.g., sorption properties, structural characteristics, reversibility, and renewability). Finally, we discussed briefly the present limitations and future prospects of these technologies.

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

New Advances in Chemical Research in 2021. Chemistry is a science major with cience and engineering. The main research directions are chemical synthesis, and research on the structure and performance of functional materials.In a patent, 57196-62-0, name is 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride, introducing its new discovery. Application of 57196-62-0

A series of alpha-glutamic acid scaffold based 4-(benzamido)-4-(1,3,4- oxadiazol-2-yl) butanoic acids were designed and synthesized as new ADAMTS inhibitors. The compounds dose-dependently inhibited the enzymatic activities of ADAMTS-4 and ADAMTS-5. One of the most active compound 2h potently inhibited ADAMTS-4 and ADAMTS-5 with IC50 values of 1.2 and 0.8 muM, respectively. These inhibitors may serve as new lead compounds for further development of therapeutics to treat osteoarthritis.

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

New Advances in Chemical Research in 2021. In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 57196-62-0, name is 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride, introducing its new discovery. Recommanded Product: 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

Two three-dimensional metal-organic frameworks, [Cd3K(L 1)6(H2O)3](OH)(DMF)4 (1) (HL1 = 3-pyrid-4-ylbenzoic acid) and [Cd(L2) 2](DMF)(H2O)0.25 (2) (HL2 = 4-pyrid-4-ylbenzoic acid), have been synthesized by using two ligands with different configuration and characterized by X-Ray diffraction and other techniques. Compound 1 shows a nanosize channel which is constructed by interlocked six-fold one-dimensional helical chains with the asymmetrical ligand HL1. Compared with compound 1, compound 2 shows a larger size channel with the symmetrical ligand HL2 in a single set of diamond cage. Nevertheless, the whole structure with the 4-fold interpenetrated diamondoid network leads to the absence of void space. The two compounds exhibit fascinating luminescence because of the interaction between Cd ions and organic ligands. The Royal Society of Chemistry 2012.

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

New Advances in Chemical Research, May 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. Product Details of 57196-62-0, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 57196-62-0, name is 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride. In an article，Which mentioned a new discovery about 57196-62-0

The title compound, poly[(mu2-formato-kappa3O,O?:O)[mu2-4-(pyridin-4-yl)benzoato-kappa3N:O,O?]zinc(II)], [Zn(C12H8NO2)(HCOO)]n, has been synthesized in situ and characterized by thermogravimetric analysis (TGA) and single-crystal and powder X-ray diffraction analyses. The polymer contains two independent structural units in the asymmetric unit. These are constructed from Zn2+ions, 4-(pyridin-4-yl)benzoate (4-pbc) bridges and in-situ-generated formate ligands, forming two similar two-dimensional (2D) layer structures. These similar 2D layers are arranged alternately and are linked with each other by dense C-H···O hydrogen bonds to generate a three-dimensional (3D) supramolecular framework. The crystal is pseudomerohedrally twinned about [201]. Compared with free 4-Hpbc, the polymer exhibits a red shift and significantly enhanced solid-state luminescence properties.

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

Chemical Research Letters, May 2021. Application of 57196-62-0, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.57196-62-0, Name is 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride, molecular formula is C10H14ClNO. In a Article，once mentioned of 57196-62-0

A 3D coordination polymer [CdK6(mu2-H2O)2(BODSDC)2(H2O)]n (1) based on the novel benzophenone-3,3?-disulfonyl-4,4?-dicarboxylate (BODSDC4?) ligand was synthesized and structurally characterized. The carboxylate and sulfonate groups of the organic ligands as well as the bridging water molecules connect the Cd2+ and K+ ions to produce a 2D layer, which is linked by the benzophenone moieties to give a 3D pillared framework. Compound 1 crystallizes in an acentric space group of Cc and has a large second-harmonic-generation (SHG) response of 1.3 times that of potassium dihydrogen phosphate (KDP) in the particle size of 25?210 mum. Further SHG measurements revealed that the material is type-I phase-matchable. The observed SHG efficiency is associated with the unsymmetrical geometry of the organic ligand and the distorted coordination polyhedrons of metal centers.

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

New research progress on 57196-62-0 in 2021. Application of 57196-62-0, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 57196-62-0, molcular formula is C10H14ClNO, introducing its new discovery.

Sulfonyl derivatives represented by the following general formula (I): Q1-Q2-T1-Q3-SO2-QAand drugs containing the same (wherein Q1is an optionally substituted, saturated or unsaturated, five- or six-membered cyclic hydrocarbon group, a five- or six-membered heterocyclic group, or the like; Q2is a single band, oxygen, sulfur, C1-C6alkylene or the like; QAis optionally substituted arylalkenyl, heteroarylalkenyl or the like; and T1is carbonyl or the like). These compounds have potent FXa-inhibitory effects and promptly exert satisfactory and persistent antithrombotic effects through oral administration, thus being useful as anticoagulant agents little accompanied with side effects.

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

Chemical Research Letters, May 2021. Research speed reading in 2021. Application In Synthesis of 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 57196-62-0, Name is 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride, molecular formula is C10H14ClNO. In a Patent，once mentioned of 57196-62-0

There is provided compounds of Formula (I) and salts, solvates, and physiologically functional derivatives thereof: wherein R1 is hydrogen or C1-6alkyl; n is 1, 2, 3 or 4; R2 is aryl, optionally substituted by one or two groups selected from the group consisting of halogen, hydroxy, cyano, C1-4alkyl, C1-4alkoxy, C1-4alkanoyl, haloC1-4alkyl, haloC1-4alkoxy, aryl, aryloxy, C1-4alkoxycarbonyl, C1-4alkylsulfonyl and a group R3R4NSO2 (wherein R3 and R4 are independently hydrogen or C1-4alkyl) and a 5- or 6-membered heteroaryl group; or n is 0 and R1 and R2, together with the nitrogen atom to which they are joined, form a 5- or 6-membered monocyclic heterocyclic ring or a 9- or 10-membered bicyclic heterocyclic ring wherein at least the ring which contains the nitrogen atom to which R1 and R2 are joined is non-aromatic, and wherein the 5- or 6-membered monocyclic heterocyclic ring or the 9- or 10-membered bicyclic heterocyclic ring is optionally substituted by one or two groups selected from the group consisting of halogen, hydroxy, cyano, oxo, C1-4alkyl, C1-4alkanoyl, C1-4alkoxy, haloC1-4alkyl, haloC1-4alkoxy, aryl, aryloxy and C1-4alkoxycarbonyl; and X is indazolyl, pyrazolyl or a group: wherein G is CH or N; and Y1 and Y2 are independently hydrogen, halogen and a group NR5R6 (wherein R5 and R6 are independently hydrogen, C1-6alkyl or C2-6alkenyl).

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

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The present invention is directed to novel compounds of formula (I) and their use in treating and/or preventing metabolic diseases

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Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem

New Advances in Chemical Research, May 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. Reference of 57196-62-0, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 57196-62-0, name is 6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride. In an article，Which mentioned a new discovery about 57196-62-0

Rigid linear compounds G1 and G2, which contained two 4-phenylpyridinium (PhPy+) units, have been prepared to investigate their binding with cucurbit[8]uril (CB[8]). X-ray crystallographic structures revealed that in the solid state both compounds were included by CB[8], through antiparallel stacking, to form 2:2 quaternary complexes (G1)2@(CB[8])2 and (G2)2@(CB[8])2. For the former complex, CB[8] entrapped G1 by holding two heterodimers of its Py+ and benzyl units, which were at opposite ends of the backbone. In contrast, for the first time, the second complex disclosed parallel stacking of two cationic Py+ units of G2 in the cavity of CB[8] in the solid state, despite the generation of important electrostatic repulsion. Isothermal titrations in water afforded high apparent association constants of 4.36×106 and 6.43×106 m?1 for 1:1 complexes G1@CB[8] and G2@CB[8], respectively, and 1H NMR spectroscopy experiments in D2O confirmed a similar stacking pattern to that observed in the solid state. A previous study and crystal structures of the 2:1 complexes formed between three new controls, G3?5, and CB[8] did not display such unusual stacking of the cationic Py+ unit; this may be attributed to the multivalency of the two CB[8] encapsulation interactions.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 57196-62-0 is helpful to your research. Reference of 57196-62-0

Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem