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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
35 Results for "
cross-coupling
" in MedChemExpress (MCE) Product Catalog:
Products (35)
35 Results for "cross-coupling" in MCE Product Catalog:
1
1 Cited Publications
Cat. No.: HY-30014
CAS No.: 348640-06-2
Cat. No.: HY-21623
CAS No.: 95464-05-4
Synonyms: TPGS-750-M
Target:
Research Areas:
DL-alpha-Tocopherol methoxypolyethylene glycol succinate (TPGS-750-M) is an amphiphile, acts as a surfactant. DL-alpha-Tocopherol methoxypolyethylene glycol succinate has a positive effect on Suzuki-Miyaura cross coupling. DL-alpha-Tocopherol methoxypolyethylene glycol succinate increases the styrene titer. DL-alpha-Tocopherol methoxypolyethylene glycol succinate is used in the stability test of NPYM-modified drugs in biological fluids .
Cat. No.: HY-W003165
CAS No.: 73583-39-8
Cat. No.: HY-W002570
CAS No.: 32316-92-0
Cat. No.: HY-W001478
CAS No.: 180695-79-8
Research Areas:
N-Boc-4-bromopiperidine is a saturated heterocyclic alkyl bromide that can be used in micelle-promoted Negishi cross-coupling reactions .
Cat. No.: HY-W033277
CAS No.: 21797-13-7
Synonyms: NSC 307191; Palladium(II) tetrafluoroborate tetraacetonitrile complex
Research Areas:
Tetrakis(acetonitrile)palladium(II) tetrafluoroborate (NSC 307191) acts as a potent Lewis acid and facilitates the formation of the 2:1 complex [Pd(1,2-bis(2′-pyridylethynyl)benzene)2](BF4)2 through the Sonogashira cross-coupling reaction.
Cat. No.: HY-W002925
CAS No.: 213697-53-1
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DavePhos is a phosphine ligand and electron donor. DavePhos can form cationic rhodium complexes to promote the selective hydrocarboxylation of styrene derivatives with CO2 and H2. As a sacrificial electron donor, DavePhos assists in generating active Rh-H species to initiate the catalytic cycle. DavePhos can be used in Buchwald−Hartwig cross-coupling reactions within palladium-based catalytic systems. DavePhos is applicable to platinum-catalyzed reductive amination of amine-acid .
Cat. No.: HY-78494
CAS No.: 13922-41-3
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1-Naphthaleneboronic acid is a biochemical reagent that can serve as a starting material or reaction reagent for chemical synthesis. 1-Naphthaleneboronic acid mainly introduces its naphthalene ring into other scaffolds through Suzuki-Miyaura cross-coupling or Friedel-Crafts alkylation reactions, thereby synthesizing target products with specific functions such as fluorescence imaging, photodynamic therapy targeting, or affinity adsorption. 1-Naphthaleneboronic acid can be used in research on photosensitizers and the synthesis of hypercrosslinked polymers with boronic acid affinity .
Cat. No.: HY-32956
CAS No.: 163105-90-6
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2-Methoxypyridine-3-boronic acid is a pyridine boronic acid compound and also borylation reagent used in Suzuki cross-coupling reactions .
Cat. No.: HY-32927
CAS No.: 150255-96-2
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3-Cyanophenylboronic acid is an arylboronic acid-based boronic acid reagent that serves as a coupling partner in Suzuki-Miyaura cross-coupling reactions. 3-Cyanophenylboronic acid participates in reactions to synthesize 4'-propoxybiphenyl-3-carbonitrile .
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5-Bromo-2-fluoropyridine is a halogenated pyridine precursor. 5-Bromo-2-fluoropyridine participates in Li-Br exchange to generate a pyridyl zinc halide for Negishi cross-coupling in the synthesis of nicotinic acetylcholine receptor agonist analogues .
Cat. No.: HY-101974
CAS No.: 1041766-91-9
Cat. No.: HY-W001194
CAS No.: 5908-62-3
Synonyms: 1,1-Dioxoisothiazolidine
Research Areas:
1,3-Propanesultam (1,1-Dioxoisothiazolidine) is a cyclic sulfonamide monomer. Polymerization of 1,3-Propanesultam under base catalysis produces high-molecular-weight polypropanesulfonamide, while polymerization under acid catalysis yields low-molecular-weight polypropanesulfonamide. 1,3-Propanesultam serves as a coupling partner in copper-catalyzed C-N cross-coupling reactions for the synthesis of 3-aminopyrazole phenylacetamide analogs. 1,3-Propanesultam is applicable to research related to organic synthesis .
Cat. No.: HY-W034801
CAS No.: 13395-16-9
Synonyms: Cupric Acetylacetonate
Target:
Research Areas:
Copper(II) acetylacetonate (Cupric Acetylacetonate) is the homoleptic acetylacetonate complex of copper(II). Copper(II) acetylacetonate is used as a catalyst in various organic reactions, including oxidation, cross-coupling, and polymerization reactions. Copper(II) acetylacetonate is also a precursor for making metal-organic frameworks (MOF) and nanomaterials .
Cat. No.: HY-W583317
CAS No.: 2375242-78-5
Research Areas:
sSPhos Pd G2 is a water-soluble palladium catalyst. sSPhos Pd G2 mediates Suzuki-Miyaura cross-coupling reactions for protein biotinylation and on-DNA reactions, thereby enabling robust gel-based ABPP using iodocysteine-reactive probes rather than bromo- or chloro-substituted probes .
Cat. No.: HY-P3350
CAS No.: 2892148-58-0
Cat. No.: HY-32928
CAS No.: 126747-14-6
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4-Cyanobenzeneboronic acid is a boronic acid derivative and also coupling reagent in Suzuki cross-coupling reactions .
Cat. No.: HY-32886
CAS No.: 168267-41-2
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Research Areas:
3,4-Difluorophenylboronic acid is an arylboronic acid that functions as a phenylating and cross-coupling reagent in palladium-catalyzed Suzuki C-C coupling reactions. 3,4-Difluorophenylboronic acid can serve as a biomaterial or organic compound for life science-related research .
Cat. No.: HY-W000873
CAS No.: 146631-00-7
Target:
Research Areas:
4-Benzyloxyphenylboronic acid is an arylboronic acid reagent that generates Monobenzone (HY-30272), a compound that inhibits melanin production in the skin, via electrochemical deboronation hydroxylation. 4-Benzyloxyphenylboronic acid serves as a coupling partner in Pd (0)-catalyzed Suzuki-Miyaura cross-coupling reactions for the synthesis of bent-core liquid crystals and liquid crystalline amphiphiles. 4-Benzyloxyphenylboronic acid is used in the study of hyperpigmentation .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
