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Nanoparticles & Nanopowders. Alternative Names: Dioxoiridium. CAS No. 12030-49-8. Molecular formula: IrO2. Mole weight: 224.22. Appearance: Black powder. Purity: 99%+. IUPACName: dioxoiridium. Density: 11.7 g/cm³. Catalog: ACM12030498-3.
Iridium (IV) Oxide
IRIDIUM (IV) OXIDE, 99.8% pure, -100 mesh, (Synonym: Iridium Dioxide), Formula: IrO2. CAS No. 12030-49-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
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Iridium(IV) oxide dihydrate
Iridium(IV) oxide dihydrate. Group: Biochemicals. Grades: Reagent Grade. CAS No. 30980-84-8. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
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Iridium (IV) Oxide, Ir 85.7%
Iridium (IV) Oxide, Ir 85.7%. CAS No. 12030-49-8. Pack Sizes: Gram Quantities: 1 gm, 5 gm. Order Number: 2034-1.
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2,2'-Bis(diphenylphosphino)biphenyl
Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones. Useful ligand for palladium-catalyzed amination and Kumada cross-coupling reactions Useful ligand for palladium-catalyzed synthesis of butatrenes. Useful ligand for iridium-catalyzed C-C cross-coupling of allenes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of dienes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation. Useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes. Ruthenium-catalyzed synthesis of indoles. Ruthenium-catalyzed oxidative cyclization. Rhodium-catalyzed boron arylation. Group: Organic phosphine compounds. Alternative Names: BIPHEP; MFCD03094574; AKOS015911364; DB-009479; 1, 1'-[[1, 1'-BIPHENYL]-2, 2'-DIYL]BIS[1, 1-DIPHENYL]-PHOSPHINE; CTK3J1519; SCHEMBL1120987; 2,2'-Bis(diphenylphosphino)biphenyl; 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl; FT-0657577. CAS No. 84783-64-2. Molecular formula: C36H28P2. Mole weight: 522.568g/mol. IUPACName: [2- (2-diphenylphosphanylphenyl) phenyl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P (C5=CC=CC=C5)C6=CC=CC=C6. Catalog: ACM84783642.
Highly active catalyst for water oxidation. Catalyst for the hydrosilylation of imines. Catalyst for C-H oxidation. Group: Iridium series of catalysts. Alternative Names: MFCD16038139; CHLORO (PENTAMETHYLCYCLOPENTADIENYL)[ (2-PYRIDINYL-KN)PHENYL-KC]IRIDUM (III); 945491-51-0. CAS No. 945491-51-0. Molecular formula: C22H31ClIrN. Mole weight: 537.164g/mol. IUPACName: carbanide;chloroiridium(2+);1,2,3,4,5-pentamethylcyclopentane;2-phenylpyridine. Canonical SMILES: [CH3-]. CC1C(C(C(C1C)C)C)C. C1=CC=C([C-]=C1)C2=CC=CC=N2. Cl[Ir+2]. Catalog: ACM945491510.
Iridium-catalyzed C-3 alkylation of oxindole with alcohols. Precursor to N-heterocyclic carbene catalyst effective for hydrogenation and alkylation of amines and alcohols. Precursor to efficient phosphine free catalyst for enantioselective hydrogenation of quinoline derivatives. Catalyst for oxidative C-H activation. Precursor to an effective water oxidation catalyst. Group: Iridium series of catalysts. Alternative Names: Dichloro (pentamethylcyclopentadienyl)iridium (III)dimer. CAS No. 12354-84-6. Molecular formula: C20H30Cl4Ir2. Mole weight: 796.7. Appearance: Orange yellow powder. Purity: 0.99. IUPACName: iridium(3+);1,2,3,4,5-pentamethylcyclopenta-1,3-diene;tetrachloride. Canonical SMILES: C[C-]1C(=C(C(=C1C)C)C)C. C[C-]1C(=C(C(=C1C)C)C)C. [Cl-]. [Cl-]. [Cl-]. [Cl-]. [Ir+3]. [Ir+3]. Catalog: ACM12354846-1.
[(R)-(+)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3-n-2-propenyl]iridium(III), min. 97%
Catalyst used for the diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol, or aldehyde, oxidation level. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxy)allylation to form anti-1,2-diols. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol, or aldehyde, oxidation level. Catalyst used for the diastereo- and enantioselective carbonyl tert-prenylation from the alcohol, or aldehyde, oxidation level. Catalyst used for the diastereo- and enantioselective carbonyl double crotylation of 1,3-diols. Catalyst used for the diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level. Group: Iridium catalysts. Alternative Names: MFCD20922908;Krische Ir Catalyst: (S)-SEGPHOS, 4-cyano-3-nitrobenzoate ligated, AldrichCPR;[(R)-(+)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3- -2-propenyl]Ir(III);[(R)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3--2-propenyl]Ir(III);1208092-27-6. CAS No. 1208092-27-6. Molecular formula: C49H36IrN2O8P2-. Mole weight: 1034.998g/mol. IUPACName: 4-cyano-3-nitrobenzene-6-ide-1-carboxylic acid; [4-(5-diphenylphosphanyl-1, 3-benzodioxol-4-yl)-1, 3-b
[(S)-(-)-5, 5'-Bis(diphenylphosphino)-4, 4'-bi-1, 3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1, 2, 3-η-2-propenyl]iridium(III), min. 97%
1. Catalyst used for the diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol, or aldehyde, oxidation level. 2. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxy)allylation to form anti-1,2-diols. 3. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol, or aldehyde, oxidation level. 4. Catalyst used for the diastereo- and enantioselective carbonyl tert-prenylation from the alcohol, or aldehyde, oxidation level. 5. Catalyst used for the diastereo- and enantioselective carbonyl double crotylation of 1,3-diols. 6. Catalyst used for the diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level. Group: Heterocyclic organic compound. CAS No. 1221768-92-8. Molecular formula: C49H35IrN2O8P2. Mole weight: 1033.98. Catalog: ACM1221768928.
Tris(2,4-pentanedionato)iridium(III)
Precursor for preparation heterogeneous catalyst on different supports for various catalytic applications: organic reactions ; water oxidation ; CO preferential oxidation ; oxygen evolution reactions; CVD/ALD precursor for preparation of Ir and Ir2O3 films on different substrates Starting material for synthesis of phosphorescent iridium complexes bearing arylpyridine ligands. Group: Micro/nanoelectronics. Alternative Names: Iridium(III) acetylacetonate, 97%; Iridium(iII)acetylacetonate; 15635-87-7; Y1427; Ir(acac)3; TRIS(ACETYLACETONATO)IRIDIUM(III); Tris(2,4-pentanedionato)iridium(III); C15H21IrO6. CAS No. 15635-87-7. Molecular formula: C15H24IrO6. Mole weight: 492.568g/mol. IUPACName: (Z)-4-hydroxypent-3-en-2-one;iridium. Canonical SMILES: CC(=CC(=O)C)O. CC(=CC(=O)C)O. CC(=CC(=O)C)O. [Ir]. ECNumber: 239-711-8. Catalog: ACM15635877.
Tris(2,4-pentanedionato)iridium(III)
Tris(2,4-pentanedionato)iridium(III). Uses: Precursor for preparation heterogeneous catalyst on different supports for various catalytic applications: organic reactions ; water oxidation ; co preferential oxidation ; oxygen evolution reactions; cvd/ald precursor for preparation of ir and ir2o3 films on different substrates starting material for synthesis of phosphorescent iridium complexes bearing arylpyridine ligands. Group: Solution deposition precursors. Alternative Names: Iridium(III) acetylacetonate, 97%; Iridium(iII)acetylacetonate; 15635-87-7; Y1427; Ir(acac)3; TRIS(ACETYLACETONATO)IRIDIUM(III); Tris(2,4-pentanedionato)iridium(III); C15H21IrO6. CAS No. 15635-87-7. Product ID: (Z)-4-hydroxypent-3-en-2-one; iridium. Molecular formula: 492.568g/mol. Mole weight: C15H24IrO6. CC(=CC(=O)C)O. CC(=CC(=O)C)O. CC(=CC(=O)C)O. [Ir]. InChI=1S/3C5H8O2. Ir/c3*1-4(6)3-5(2)7; /h3*3, 6H, 1-2H3; /b3*4-3-;. AZFHXIBNMPIGOD-LNTINUHCSA-N.
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