Category: iodides-buliding-blocks

Hibe, Yuta published the artcileOn spin-lattice relaxation of nuclear quadrupole resonance in polycrystalline solids, SDS of cas: 6443-90-9, the publication is Chemical Physics Letters (2022), 139379, database is CAplus.

The anal. of spin-lattice relaxation in NQR (NQR) of spin-(5/2) reported by Okubo and Igarashi (Z. Naturforsch. A. 56 (2001) 777) is extended to take account of the distribution of the initial non-equilibrium populations created by a resonant radio-frequency pulse in powder. The proposed theory is applicable to axially sym. elec. field gradient tensor and is examined for spin-lattice relaxation of ¹²⁷I NQR in polycrystalline pyridine iodine monochloride measured at 469 MHz at 77 K.

Chemical Physics Letters published new progress about 6443-90-9. 6443-90-9 belongs to iodides-buliding-blocks, auxiliary class Pyridines, name is Pyridine Iodochloride complex, and the molecular formula is C5H5ClIN, SDS of cas: 6443-90-9.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Koike, Takeshi published the artcileTotal synthesis of racemic ligularone and isoligularone, Computed Properties of 31253-08-4, the publication is Chemical & Pharmaceutical Bulletin (1999), 47(6), 897-899, database is CAplus.

Racemic ligularone (I) and isoligularone (II) were synthesized from the cis-4aβ,5,6,7,8,8a-hexahydro-8β,8aβ-dimethylnaphthalene-1,3(2H,4H)-dione (III) by furannulation reaction with diethyl(prop-2-ynyl)sulfonium bromide, prepared from di-Et sulfide and propargyl bromide.

Chemical & Pharmaceutical Bulletin published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C5H9IO2, Computed Properties of 31253-08-4.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Bowmaker, Graham A. published the artcileVibrational spectra of adducts of iodine monochloride with some pyridine bases, Safety of Pyridine Iodochloride complex, the publication is Australian Journal of Chemistry (1980), 33(8), 1743-51, database is CAplus.

A series of mol. adducts, L-ICl, where L = pyridine or a pyridine derivative, were prepared and the solid state spectra examined by Raman and far-IR spectroscopy. Assignments of the modes ν(I-Cl) 240-300 cm^-1 and ν(N-I) 90-180 cm^-1 and force constant calculations in a simple 3-center model yield information on structure and bonding related to the nature of the pyridine donor. Several ionic products containing the ICl₂^– ion were encountered.

Australian Journal of Chemistry published new progress about 6443-90-9. 6443-90-9 belongs to iodides-buliding-blocks, auxiliary class Pyridines, name is Pyridine Iodochloride complex, and the molecular formula is C5H5ClIN, Safety of Pyridine Iodochloride complex.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Reeves, Jonathan T. published the artcileCopper-catalyzed annulation of 2-formylazoles with aminoiodopyrazoles: Synthesis of new heterocyclic ring systems, Name: 4-Iodo-1-methyl-1H-pyrazol-5-amine, the publication is Journal of Heterocyclic Chemistry (2013), 50(3), 680-683, database is CAplus.

Various 2-formyl azoles underwent CuI/sparteine-catalyzed annulation with 1-substituted 4-iodo-5-aminopyrazoles to produce pyrazolo[3,4-e]pyrrolo[1,2-a]pyrazines and imidazo[1,2-a]pyrazolo[3,4-e]pyrazines. The reaction was demonstrated for 2-formylpyrroles, 2-formylindoles, 2-formylimidazole, and 3-methyl-5-formylpyrazole. 3-Substitution of the iodopyrazole was tolerated.

Journal of Heterocyclic Chemistry published new progress about 1443278-79-2. 1443278-79-2 belongs to iodides-buliding-blocks, auxiliary class Pyrazole,Iodide,Amine, name is 4-Iodo-1-methyl-1H-pyrazol-5-amine, and the molecular formula is C4H6IN3, Name: 4-Iodo-1-methyl-1H-pyrazol-5-amine.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Konishi, Hideyuki published the artcilePd-Catalyzed Selective Synthesis of Cyclic Sulfonamides and Sulfinamides Using K₂S₂O₅ as a Sulfur Dioxide Surrogate, SDS of cas: 500563-90-6, the publication is Organic Letters (2017), 19(7), 1578-1581, database is CAplus and MEDLINE.

A variety of cyclic sulfonamides and sulfinamides could be selectively synthesized under Pd catalysis using haloarenes bearing amino groups and a sulfur dioxide (SO₂) surrogate. The amount of base was key in determining the selectivity. Mechanistic studies revealed that sulfinamides were initially formed via an unprecedented formal insertion of sulfur monoxide and were oxidized to sulfonamides in the presence of an iodide ion and DMSO.

Organic Letters published new progress about 500563-90-6. 500563-90-6 belongs to iodides-buliding-blocks, auxiliary class Nitro Compound,Iodide,Benzene,Alcohol, name is (2-Iodo-4-nitrophenyl)methanol, and the molecular formula is C7H6INO3, SDS of cas: 500563-90-6.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Zhang, Dejiang published the artcileNickel- and Palladium-Catalyzed Cross-Coupling of Stibines with Organic Halides: Site-Selective Sequential Reactions with Polyhalogenated Arenes, COA of Formula: C6H13I, the publication is ACS Catalysis (2022), 12(2), 854-867, database is CAplus.

Herein, the authors disclose a general and efficient method for the synthesis of Sb-aryl and Sb-alkyl stibines by the Ni-catalyzed cross-coupling of halostibines with organic halides. The synthesized Sb-aryl stibines couple with aryl halides to give biaryls efficiently via Pd catalysis. Sequential reactions of stibines with polyhalogenated arenes bearing active C-I/C-Br sites and inactive C-Cl sites successfully proceeded, giving a variety of complex mols. with good site selectivity. Drugs such as diflunisal and fenbufen, as well as a fenofibrate derivative, were synthesized on gram scales in good yields, together with the high recovery of chlorostibine. Also, catalytic mechanisms are proposed based on the results of control experiments

ACS Catalysis published new progress about 638-45-9. 638-45-9 belongs to iodides-buliding-blocks, auxiliary class Iodide,Aliphatic hydrocarbon chain, name is 1-Iodohexane, and the molecular formula is C5H7F3O3, COA of Formula: C6H13I.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Lei, Lin published the artcileSystematic Study on Alkyl Iodide Initiators in Living Radical Polymerization with Organic Catalysts, HPLC of Formula: 31253-08-4, the publication is Macromolecules (Washington, DC, United States) (2014), 47(19), 6610-6618, database is CAplus.

Several low-molar-mass alkyl iodides were studied as initiating dormant species in living radical polymerization with organic catalysts. Primary, secondary, and tertiary alkyl iodides with different stabilizing groups (ester, Ph, and cyano groups) were systematically studied for the rational design of initiating alkyl iodides. The activation rate constants of these alkyl iodides were exptl. determined for quant. comparison. These alkyl iodides were used in the polymerizations of Me methacrylate and Bu acrylate to examine their initiation ability in these polymerizations A telechelic polymer was prepared using an alkyl iodide with a functional group. Alkyl iodides with multi-initiating sites were also studied.

Macromolecules (Washington, DC, United States) published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C5H9IO2, HPLC of Formula: 31253-08-4.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Kamiya, Naoshi published the artcileDehalogenation of α-halo carbonyl compounds by a new efficient reagent, triphenylphosphonium iodide, Recommanded Product: Ethyl 2-Iodopropionate, the publication is Chemistry Letters (1992), 293-6, database is CAplus.

Ph₃PHI is an efficient reagent for the dehalogenation of α-halo carbonyl compounds, e.g., MeCHClAc to EtAc. α-Halo esters, which were difficult to reduce with Me₃SiCl/NaI reagent, were smoothly debrominated by Ph₃PHI. Treatment of α-halo carbonyl compounds with Ph₃PDI produced the corresponding α-deuterated compounds

Chemistry Letters published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C5H9IO2, Recommanded Product: Ethyl 2-Iodopropionate.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Since, Marc published the artcileOriginal TDAE strategy using α-halocarbonyl derivatives, Name: Ethyl 2-Iodopropionate, the publication is Tetrahedron (2009), 65(31), 6128-6134, database is CAplus.

The selective C-C bond formation by the reaction of nitrobenzyl carbanions, formed via the TDAE strategy, with α-haloesters and α-haloamides is disclosed. This reaction, extended in benzodioxole and dimethoxybenzene series provides new potentially CNS active agents.

Tetrahedron published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C15H21BO2, Name: Ethyl 2-Iodopropionate.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Takale, Balaram S. published the artcileMild and Robust Stille Reactions in Water using Parts Per Million Levels of a Triphenylphosphine-Based Palladacycle, Synthetic Route of 602303-26-4, the publication is Angewandte Chemie, International Edition (2021), 60(8), 4158-4163, database is CAplus and MEDLINE.

An inexpensive and new triphenylphosphine-based palladacycle has been developed as a pre-catalyst, leading to highly effective Stille cross-coupling reactions in water under mild reaction conditions. Only 500-1000 ppm of Pd suffices for couplings involving a variety of aryl/heteroaryl halides with aryl/hetaryl stannanes. Several drug intermediates can be prepared using this catalyst in aqueous nanoreactors formed by 2 wt % Brij-30 in water.

Angewandte Chemie, International Edition published new progress about 602303-26-4. 602303-26-4 belongs to iodides-buliding-blocks, auxiliary class Other Aromatic Heterocyclic,Chloride,Iodide, name is 7-Chloro-2-iodothieno[3,2-b]pyridine, and the molecular formula is C8H15ClN2, Synthetic Route of 602303-26-4.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com