Category: tetrahydroisoquinoline

Formula: C10H10Cl2N2Pt. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: cis-Dichlorobis(pyridine)platinum(II), is researched, Molecular C10H10Cl2N2Pt, CAS is 15227-42-6, about Mass spectrometry of cis-platin in urine.

The mass spectra of cisplatin  [15663-27-1] and its analogs are presented. A urine sample of a cancer patient treated with cisplatin was extracted with 0.1N-HCl and then washed with COMe2/CHCl3. The component containing Pt was eluted with 2N-HBr using an ion exchange chromatog. technique. The mass spectrum of the component showed the change from Cl-type to Br-type as the unchanged type of carrier ligand. Thus, mass spectrometry may be a useful method to elucidate the action mechanism of cisplatin.

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

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: Picolinamide( cas:1452-77-3 ) is researched.Computed Properties of C6H6N2O.Ren, Shishuai; Wang, Yangyang; Yang, Fei; Sun, Hongjian; Li, Xiaoyan published the article 《Dehydration of primary amides to nitriles catalyzed by [CNC]-pincer hydrido cobalt(III) complexes》 about this compound( cas:1452-77-3 ) in Catalysis Communications. Keywords: amide nitrile cobalt hydride catalyst dehydration selective safety; nitrile preparation. Let’s learn more about this compound (cas:1452-77-3).

The dehydration reactions from primary amides to nitriles were catalyzed by the [CNC]-pincer hydrido cobalt(III) complexes [(ortho-F4C6-CH=N-C10H6)Co(III)(H)(PMe3)2], [(2,5-F2C6H2-CH=N-C10H6)Co(III)(H)(PMe3)2] (I) and [(2,4,5-F3C6H-CH=N-C10H6)Co(III)(H)(PMe3)2] as catalysts with (EtO)3SiH as an efficient reducing agent. These hydrido cobalt(III) complexes as catalysts are suitable for many substrates and have good functional group tolerance. Among the three cobalt hydrides, complex I is the best catalyst. This is the first hydrido cobalt complex-catalyzed dehydration of primary amides to nitriles.

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

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 1-Bromoundecane, is researched, Molecular C11H23Br, CAS is 693-67-4, about Synthesis and biological evaluation of novel bis-quaternary ammonium compounds with p-terphenyl spacer, the main research direction is quaternary ammonium compound terphenyl spacer preparation SAR; antibacterial antifungal cytotoxicity human.Related Products of 693-67-4.

Bis-quaternary ammonium compounds I·2 Br- [R = H(CH2)n; n = 7, 8, 9, 10, 11] with a p-terphenyl spacer between two pyridinium heads were synthesized. I·2 Br- (n = 8) was superior to the known benzalkonium chloride, miramistin and chlorhexidine bisgluconate in its MIC values against five pathogenic bacteria.

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Tetrahydroisoquinoline – Wikipedia,
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Reference of Picolinamide. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: Picolinamide, is researched, Molecular C6H6N2O, CAS is 1452-77-3, about Direct Synthesis of Alternating Polycarbonates from CO2 and Diols by Using a Catalyst System of CeO2 and 2-Furonitrile. Author is Gu, Yu; Matsuda, Keitaro; Nakayama, Akira; Tamura, Masazumi; Nakagawa, Yoshinao; Tomishige, Keiichi.

The control technique of polymer mol. weight is required for the synthesis of versatile polymers with various properties. In our previous work, we found that CeO2 + 2-cyanopyridine catalyst system was effective for the direct synthesis of alternating polycarbonates from CO2 and diols, however, the maximum average mol. weight was ∼1000 g mol-1 (d.p. = 7-8). In this study, we succeeded in the synthesis of alternating polycarbonates with higher mol. weight from CO2 and diols by using a catalyst system of CeO2 + 2-furonitrile. The average mol. weight reached up to 5000 g mol-1 and could be controlled by adjusting the amount of diols and 2-furonitrile. Moreover, polycarbonate diols, polycarbonates without capping of OH groups at the ends, were obtained with the average mol. weight of ∼2000 g mol-1. The catalyst system was applicable to the direct polymerization of CO2 and various α,ω-diols, providing the corresponding alternating polymers. Comparison of CeO2 + 2-cyanopyridine and CeO2 + 2-furonitrile catalyst systems based on the kinetics and DFT calculations showed two main causes for the formation of polycarbonates with higher mol. weight in the CeO2 + 2-furonitrile catalyst system: First, the reactivity of 2-furamide, which was formed from 2-furonitrile, with produced polycarbonate diols was lower than that of 2-picolinamide, which was formed from 2-cyanopyridine, leading to decrease of formation of ester-capped polycarbonates. Second, the adsorption of 2-furonitrile on CeO2 was weaker than that of 2-cyanopyridine, leading to low steric hindrance at the active sites of CeO2 and enabling the reaction of longer diols, such as polycarbonate diols with CO2.

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

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: D-Alanine methylamide hydrochloride( cas:61302-99-6 ) is researched.Application In Synthesis of D-Alanine methylamide hydrochloride.Zhang, Xiaofei; Ligny, Romain; Chewchanwuttiwong, Sopa; Hadade, Rawan; Laurent, Mathieu Y.; Martel, Arnaud; Jacquemmoz, Corentin; Lhoste, Jerome; Bricaud, Sullivan; Py, Sandrine; Dujardin, Gilles published the article 《δ-Valerolactamic quaternary amino acid derivatives: Enantiodivergent synthesis and evidence for stereodifferentiated β-turn-inducing properties》 about this compound( cas:61302-99-6 ) in Journal of Organic Chemistry. Keywords: valerolactamic quaternary amino acid enantiodivergent synthesis peptidomimetic beta turn; pseudopeptide synthesis conformer steric hindrance crystal mol structure DFT; isoxazolidine pentenoyl protection reductive ring opening reduction oxidation; reductive amination cyclization peptide coupling. Let’s learn more about this compound (cas:61302-99-6).

Enantiopure (R) and (S) cyclic α,α-disubstituted amino acid derivatives displaying a δ-valerolactam side chain were prepared from a common isoxazolidine precursor. The (R)-configured δ-valerolactam (I) was converted into diastereoisomeric pseudopeptides to investigate its ability to induce secondary structures in peptidomimetics. Conformational studies of these pseudopeptides were carried out in the solid state (X-ray diffraction), in solution (NMR analyses), and in silico (computer-aided conformational anal.), which demonstrated that such quaternary amino acids induce β-turn conformations stable enough to be retained in polar media (DMSO). Incorporation of this new type of α,α-disubstituted amino acid into a representative pseudopeptidic sequence by N- then C-elongation and N-debenzylation is also described herein and could serve for the synthesis of various structured peptidomimetics.

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Rieth, Thorsten; Tober, Natalie; Limbach, Daniel; Haspel, Tobias; Sperner, Marcel; Schupp, Niklas; Wicker, Philipp; Glang, Stefan; Lehmann, Matthias; Detert, Heiner published an article about the compound: 1-Bromoundecane( cas:693-67-4,SMILESS:CCCCCCCCCCCBr ).Application In Synthesis of 1-Bromoundecane. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:693-67-4) through the article.

Tristriazolotriazines with a threefold alkoxyphenyl substitution were prepared and studied by DSC, polarized optical microscopy (POM) and X-ray scattering. Six pentyloxy chains are sufficient to induce liquid-crystalline behavior in these star-shaped compounds Thermotropic properties of tristriazolotriazines with varying substitution patterns and a periphery of linear chains of different lengths, branching in the chain and swallow-tails, are compared. Generally, these disks display broad and stable thermotropic mesophases, with the tangential tristriazolotriazines being superior to the radial isomer. The structure-property relationships of the number of alkyl chains, their position, length and structure were studied.

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Tetrahydroisoquinoline – Wikipedia,
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So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Tomishige, Keiichi; Tamura, Masazumi; Nakagawa, Yoshinao researched the compound: Picolinamide( cas:1452-77-3 ).Safety of Picolinamide.They published the article 《CO2 Conversion with Alcohols and Amines into Carbonates, Ureas, and Carbamates over CeO2 Catalyst in the Presence and Absence of 2-Cyanopyridine》 about this compound( cas:1452-77-3 ) in Chemical Record. Keywords: carbonate urea carbamate catalyst cyanopyridine cerium oxide; Carbamate; Carbon dioxide; Cerium oxide; Organic carbonate; Urea. We’ll tell you more about this compound (cas:1452-77-3).

Recent progress on the CeO2 catalyzed synthesis of organic carbonates, urea, and carbamates from CO2+alcs., CO2+amines, and CO2+alcs.+amines, resp., is reviewed. The reactions of CO2 with alcs. and amines are reversible ones and the degree of the equilibrium limitation of the synthesis reactions is strongly dependent on the properties of alcs. and amines as the substrates. When the equilibrium limitation of the reaction is serious, the equilibrium conversion of the substrate and the yield of the target product is very low, therefore, the shift of the equilibrium reaction to the product side by the removal of H2O is essential in order to get the target product in high yield. One of the effective method of the H2O removal from the related reaction systems is the combination with the hydration of 2-cyanopyridine to 2-picolinamide, which is also catalyzed by CeO2.

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

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 1-Bromoundecane, is researched, Molecular C11H23Br, CAS is 693-67-4, about Ionic liquid crystals: Synthesis and characterization via NMR, DSC, POM, X-ray diffraction and ionic conductivity of asymmetric viologen bistriflimide salts.Reference of 1-Bromoundecane.

A series of asym. viologen bistriflimide salts I (R = n-pentyl, dodecyl, octadecyl, etc.) of both short and long alkyl chains were synthesized by the metathesis reaction of lithium triflimide salt with the resp. asym. viologen dibromide salts II in methanol. Their thermotropic liquid crystalline properties were determined by differential scanning calorimetry, polarizing optical microscopy and variable temperature X-ray diffraction techniques. These salts melt into highly-ordered smectic T phases i.e., crystal-to SmT transitions (Tms) at relatively low temperatures (lowest Tm at -12°C) and maintain liquid crystallinity in a wide range of temperatures (8-132°C), with excellent thermal stabilities up to 320°C as determined by thermogravimetric anal. These results differ with respect to the sym. viologen bistriflimide salts I. Ionic conductivity of these salts was also measured by dielec. impedance spectroscopy and found to be in the 10-2.5 S cm-1 range, highlighting their potential as electrolytes at room temperature

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Category: tetrahydroisoquinoline. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 4-Amino-2-(tert-butyl)pyrimidine, is researched, Molecular C8H13N3, CAS is 114362-20-8, about σ-Adduct formation between amines and liquid ammonia. Part 47. On the Chichibabin amination of pyrimidine and N-alkylpyrimidinium salts using liquid ammonia/potassium permanganate. Author is Buurman, Dick J.; Van der Plas, Henk C..

4-Aminopyrimidines I (R1 = C1-4 alkyl) and iminodihydropyrimidines II (R2 = Et, CHMe2) were prepared 2-Alkylpyrimidines were treated with KNH2-NH3-KMnO4 to give I. The reaction of 1,2-diethylpyrimidinium fluoroborate with NH3-KMnO4 gave II (R2 = Et).

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In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Luminescence properties of some platinum(II) complexes. Counter-ion and molecular geometry effects, published in 1973, which mentions a compound: 15227-42-6, Name is cis-Dichlorobis(pyridine)platinum(II), Molecular C10H10Cl2N2Pt, SDS of cas: 15227-42-6.

Reflectance and luminescence spectra, and emission lifetimes of 14 charged and neutral Pt(II) crystalline complexes are reported. The lifetimes (in the range of some tens of μsec) indicate that the emissions are due to a spin-forbidden process. On the basis of spectral correlations, the phosphorescence is tentatively identified as due to the lowest d-d ligand field transition when the bonding of the ligand is essentially σ in character, and to a π* → d charge-transfer transition for those complexes in which the ligands themselves have π orbital systems. Both the radiative (kr) and nonradiative (kn) rate constants are sensitive to changes in mol. geometry (cis,trans isomers) and counter-ions. By assuming unitary efficiency for the intersystem crossing to the emitting state, the counter-ion appears to predominantly affect kn through vibrational coupling of the chromophore with the lattice. For the cis forms, both kr and kn are affected in a complex manner, with metal-metal interactions playing an important role. For the trans forms, however, the constancy of the quantum yield with respect to temperature suggests that kn is negligible in comparison to kr, and therefore the trans chromophores behave as isolated systems within the crystalline lattice.

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Tetrahydroisoquinoline – Wikipedia,
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