Propargyl Alcohol Suppliers USA
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Product | Description | |
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Propargyl Alcohol Quick inquiry Where to buy Suppliers range | Propargyl Alcohol is used as a corrosion inhibitor, a metal complex solution, a solvent stabilizer and an electroplating brightener additive. It is also used as an intermediate in organic synthesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 107-19-7. Pack Sizes: 10ml, 50ml. Molecular Formula: C3H4O. US Biological Life Sciences. | Worldwide |
Propargyl alcohol propoxylate Quick inquiry Where to buy Suppliers range | Propargyl alcohol propoxylate. Group: Nickel Plating Intermediates. Alternative Names: 2-(Prop-2-yn-1-yloxy)propan-1-ol. CAS No. 3973-17-9. IUPAC Name: 2-Prop-2-ynoxypropan-1-ol. Molecular Weight: 114.14. Molecular Formula: C6H10O2. SMILES: CC(CO)OCC#C. Flash Point: 50%+. | |
Propargyl Alcohol-13C3 Quick inquiry Where to buy Suppliers range | Propargyl Alcohol-13C3 is labelled Propargyl Alcohol which is used as a corrosion inhibitor, a metal complex solution, a solvent stabilizer and an electroplating brightener additive. It is also used as an intermediate in organic synthesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 201740-99-0. Pack Sizes: 10mg, 100mg. Molecular Formula: 13C3H4O, Molecular Weight: 59.04. US Biological Life Sciences. | Worldwide |
Propargyl Alcohol-13C3 Quick inquiry Where to buy Suppliers range | Propargyl Alcohol-13C3. Uses: For analytical and research use. Group: Enzyme Activators, Inhibitors & Substrates. Alternative Names: Prop-2-yn-1-ol 13C3. CAS No. 201740-99-0. Pack Sizes: 10MG. IUPAC Name: (1,2,3-^{13}C_{3})prop-2-yn-1-ol. Molecular formula: 13C3H4O. Mole weight: 59.04. Catalog: APS201740990. SMILES: O[13CH2][13C]#[13CH]. Format: Neat. Product Type: Stable Isotope Labelled. Shipping: Room Temperature. | |
Propargyl-PEG3-alcohol Quick inquiry Where to buy Suppliers range | Propargyl-PEG3-alcohol. Group: Other PEG Linkers. Grades: 95%+. CAS No. 208827-90-1. Product ID: ACM208827901. Molecular formula: C9H16O4. Mole weight: 188.22. | |
1,3,5-Benzenetricarbonyl Trichloride Quick inquiry Where to buy Suppliers range | 1,3,5-Benzenetricarbonyl trichloride reacts with propargyl alcohol to yield triprop-2-ynyl benzene-1,3,5-tricarboxylate. Uses: 1,3,5-Benzenetricarbonyl trichloride was used in the synthesis of chiral azoaromatic dendrimeric systems. It was used to study the structure of activated composite membranes containing organophosphorus extractants as carriers. It was the starting material for two tritopic amides derived from 3- and 4-methylaminopyridine which self-assembled into nanoballs on treatment with palladium(II) nitrate in DMSO. Group: Halogen Functional Groups. Alternative Names: Trimesoyl chloride, Benzene-1,3,5-tricarbonyl chloride, Trimesic acid trichloride. CAS No. 4422-95-1. Molecular Weight: 265.48. Molecular Formula: C6H3(COCl)3. SMILES: ClC(=O)c1cc(cc(c1)C(Cl)=O)C(Cl)=O. Flash Point: 98%. | |
2-Hexyn-1-ol Quick inquiry Where to buy Suppliers range | 2-Hexyn-1-ol is a propargyl alcohol that is naturally found as a volatile fragrance component of chestnut blossoms. 2-Hexyn-1-ol also has potential antifungal properties against Aspergillus oryzae, a fungus that is used to produce fermented foods and beverages in Japan. Group: Biochemicals. Grades: Highly Purified. CAS No. 764-60-3. Pack Sizes: 2.5g, 10g. Molecular Formula: C6H10O, Molecular Weight: 98.14. US Biological Life Sciences. | Worldwide |
2-Nonyn-1-ol Quick inquiry Where to buy Suppliers range | 2-Nonyn-1-ol is a Propargyl alcohol (P762550) derivative that is used as a reagent to synthesize Microcarpalide, a microfilament disrupting agent that is weakly cytotoxic to mammalian cells. 2-Nonyn-1-ol is also thought to have potential antifungal properties. Group: Biochemicals. Grades: Highly Purified. CAS No. 5921-73-3. Pack Sizes: 1g, 5g. Molecular Formula: C9H16O, Molecular Weight: 140.22. US Biological Life Sciences. | Worldwide |
3-(tert-Butyldimethylsilyloxy)-1-propyne Quick inquiry Where to buy Suppliers range | An alkyne used in organinc synthesis. Group: Biochemicals. Alternative Names: 1-(tert-Butyldimethylsilyloxy)-2-propyne; 1-tert-Butyldimethylsiloxy-2-propyne; 3-(Dimethyl-tert-butylsiloxy)propyne; 3- (tert-Butyldimethylsiloxy) propyne; 3-(tert-Butyldimethylsilyloxy)-1-propyne; 3- (tert-Butyldimethylsilyloxy) propyne; 3-tert-Butyldimethylsiloxy-1-propyne; Dimethyl(2-Propynyloxy)(tert-butyl)silane; Propargyl Alcohol tert-Butyldimethylsilyl ether; tert-Butyldimethyl(2-propyn-1-yloxy)silane; tert-Butyldimethyl(2-propynyloxy)silane; tert-Butyldimethylsilyl Propargyl Ether. Grades: Highly Purified. CAS No. 76782-82-6. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
3-(Trimethylsilyl)-2-propyn-1-ol Quick inquiry Where to buy Suppliers range | Transparent liquid. Group: Silanols. Alternative Names: 3-trimethylsilylprop-2-yn-1-ol; 3-(Trimethylsilyl)propargyl Alcohol; 3-TriMethylsilyl-2-propyn-1-ol. Grades: 95%+. CAS No. 5272-36-6. Molecular formula: C6H12OSi. Mole weight: 128.24. IUPAC Name: 3-trimethylsilylprop-2-yn-1-ol. Exact Mass: 128.06600. EC Number: 226-094-5. Boiling Point: 76ºC (20 mmHg). Flash Point: 66ºC. Density: 0.865. SMILES: C[Si](C)(C)C#CCO. InChIKey: ZVGCJDPEKKEYES-UHFFFAOYSA-N. Safty Description: S26-S37/39. Hazard statements: Xi: Irritant. | |
6,7-Dihydro-2-phenyl-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride, min. 98% Quick inquiry Where to buy Suppliers range | 6,7-Dihydro-2-phenyl-5H-pyrrolo[2,1-c]-1,2,4-triazolium chloride, min. 98%. Uses: Reagent used for the conversion of α-haloaldehydes into acylating agents via a catalyzed internal redox reaction. Reagent used for reduction of styryl and propargylic alcohols. Catalyst for the synthesis of 3-substituted phthalides. Group: Heterocyclic Organic Compound. Alternative Names: 828914-68-7;CTK5F0182;DTXSID40722618;5H-Pyrrolo[2,1-c]-1,2,4-triazoliuM,6,7-dihydro-2-phenyl-,chloride;2-Phenyl-1,2,3,5,6,7-hexahydropyrrolo[2,1-c][1,2,4]triazol-4-ium chloride;5H-Pyrrolo[2,1-c]-1,2,4-triazolium,6,7-dihydro-2-phenyl-, chloride (1:1). CAS No. 828914-68-7. Molecular formula: C11H14ClN3. Mole weight: 223.704g/mol. IUPAC Name: 2-phenyl-3,5,6,7-tetrahydro-1H-pyrrolo[2,1-c][1,2,4]triazol-4-ium;chloride. Rotatable Bond Count: 1. Exact Mass: 223.088g/mol. SMILES: C1CC2=[N+](C1)CN(N2)C3=CC=CC=C3.[Cl-]. InChI: InChI=1S/C11H13N3.ClH/c1-2-5-10(6-3-1)14-9-13-8-4-7-11(13)12-14;/h1-3,5-6H,4,7-9H2;1H. InChIKey: FRPZAASMSPGXLF-UHFFFAOYSA-N. H-Bond Donor: 1. H-Bond Acceptor: 2. Monoisotopic Mass: 223.088g/mol. | |
(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) Quick inquiry Where to buy Suppliers range | (9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine). Uses: Ligand used for the hydroformylation of alkenes. Ligand used in the intermolecular coupling of amides and hydrazones with aryl halides. Ligand used in the intermolecular coupling of amides with aryl halides or triflates. Ligand used in the coupling of heteroarylamines and aryl halides. Ligand used in the hydrophosphinylation of alkenes and alkynes. Ligand used for the Au(I)-catalyzed dehydrogenative silation of alcohols. Ligand used for the sulfinylation of aryl iodides. Ligand used for the Pd-catalyzed carbonylation reaction of aryl bromides and amines. Ligand used for the Ni-cataltzed alkynylcyanation of alkynes. Ligand used for the Pd-catalyzed N-arylation of 3-amino-1H-pyrazole. Ligand used for the Rh-catalyzed dehydrogenation borylation of cyclic alkenes. Ligand used for the Pd-catalyzed intermolecular coupling of H-Phosphonate diesters with benzyl halides. Ligand used for the Pd-catalyzed one pot synthesis of 4-aryl-1H-1,2,3-triazoles. Ligand used for the Pd-catalyzed intermolecular addition of formamides to alkynes. Ligand used for the Pd-catalyzed decarboxylative couplings of 2-(2-azaaryl)acetates with aryl halides and triflates. Ligand used for the Pd-catalyzed benzylic arylation of 2-methyl azaarenes Ligand used for the Pd-catalyzed α-arylation of heteroaromatic ketones. Ligand used for the Pd-catalyzed direct alkynlation of both azoles and azolines. Ligand used for the Cu-catalyzed intermolecular coupling of alkynes with aryl iodides. Ligand used for the Pd-catalyzed ene-type reaction of aldehydes with 1,3-diene. Ligand used for the Ru-catalyzed intermolecular addition of 2-phenylbenzoic acid onto unactivated olefins. Ligand used for the Pd/Cu-catalyzed direct arylation of heteroarenes. Ligand used for the Pd-catalyzed reaction of propargyl-substituted malonate esters with aryl halides. Ligand used for the Pd-catalyzed decarboxylative coupling of tertiary cyanoacetate salts with aryl halides and triflates. Ligand used for the Pd-catalyzed hydroesterification of alkynes. Ligand used for the Cu-catalyzed arylation of arylboronic acids with aldehydes. Ligand used for the Ru-catalyzed oxidative synthesis of heterocycles from alcohols. Ligand used for the Rh-catalyzed borylation of ni | |
Alkyne-PEG5-OH Quick inquiry Where to buy Suppliers range | Alkyne-PEG5-OH. Group: PEG Derivatives. Alternative Names: Propargyl-PEG7-OH;Propargyl-PEG7-alcohol;3,6,9,12,15,18,21-Heptaoxatetracos-23-yn-1-ol. CAS No. 1036204-60-0. Product ID: MD007002-5. | |
Bis(cyclopentadienyl)zirconium chloride hydride (Schwartz's Reagent), 95% Quick inquiry Where to buy Suppliers range | Bis(cyclopentadienyl)zirconium chloride hydride (Schwartz's Reagent), 95%. Uses: Reagent for the hydrozirconation of olefins. Reagent for the hydrozirconation of alkynes. Catalyst for the hydroboration of olefins. Mediates the reduction of tertiary amides to aldehydes, without reduction of cyano, nitro, ester, or α,β-unsaturated groups. Catalyst for the asymmetric vinylation and dienylation of ketones. Useful reagent for dimethylzinc mediated additions alkenylzirconocenes to aldimines. Useful reagent for the synthesis of oxidized amides from nitriles. Reagent for the hydrozirconation of propargylic alcohols. Group: Organic Phosphine Compounds. Alternative Names: 37342-97-5; bis (cyclopentdienyl)zirconium (IV)chloride hydride; TR-015164; RTR-015164; FT-0696293. CAS No. 37342-97-5. Molecular formula: C10H11ClZr. Mole weight: 257.872g/mol. IUPAC Name: cyclopenta-1, 3-diene; hydride; zirconium(4+); chloride. Exact Mass: 255.96g/mol. EC Number: 253-479-5. SMILES: [H-].C1C=CC=[C-]1.C1C=CC=[C-]1.[Cl-].[Zr+4]. InChI: InChI=1S/2C5H5.ClH.Zr.H/c2*1-2-4-5-3-1;;;/h2*1-3H,4H2;1H;;/q2*-1;;+4;-1/p-1. InChIKey: WIKZVPGVVYRJLQ-UHFFFAOYSA-M. H-Bond Acceptor: 4. Monoisotopic Mass: 255.96g/mol. | |
Ethyl propiolate Quick inquiry Where to buy Suppliers range | Ethyl propiolate. Group: Pheromone Ingredients. Alternative Names: Ethyl propiolate;623-47-2;ethyl prop-2-ynoate;2-Propynoic acid, ethyl ester;Ethyl acetylenecarboxylate;ETHYL PROPYNOATE;Propiolic acid ethyl ester;Ethyl 2-propynoate; (Ethoxycarbonyl)acetylene; Propiolic acid, ethyl ester;MFCD00009184;UNII-W235G5U52S;Ethyl propiolate, 99%;Propynoic Acid Ethyl Ester;Propargylic Acid Ethyl Ester;CHEBI:51740;W235G5U52S;2-propynoic acid ethyl ester;ethyl propalate;ethyl propioloate;ethanol propiolate;ethyl propargylate;ethyl propio late;ethyl propio-late;Ethyl propiolate;;ethyl-2-propynate;EINECS 210-795-8;PubChem4070;ethyl [2H]-propiolate;AI3-37704;ACMC-209n2h;CHEMBL53384;prop-2-ynoic acid ethyl ester; DTXSID80211359; ACN-S004046; ACT08916; ALBB-013040; NSC60551; STR01248; ZINC1690295; ANW-34167; BBL104247; NSC-60551; RW2104; SBB060344; STL197580; AKOS005173738; MCULE-3783424133; AK-73085; H399; ACETYLENECARBOXYLIC ACID ETHYL ESTER;AB0013032;AM20100525;BB 0258015;CS-0015842;FT-0625791;FT-0695777;P0529;ST51046542;C-4829;13896-EP2308838A1;13896-EP2316836A1;38055-EP2272509A1;38055-EP2289871A1;38055-EP2298750A1;38055-EP2305629A1;38055-EP2311796A1;38055-EP2311797A1;38055-EP2311798A1;38055-EP2311799A1;A833725;A1-01104;J-521279;J-802201;Q27122726;F0001-1671;59938-67-9. Grades: N/A. CAS No. 623-47-2. Molecular formula: C5H6O2. Mole weight: 98.10g/mol. IUPAC Name: ethyl prop-2-ynoate. EC Number: 210-795-8. Boiling Point: 120.0 °C. Solubility: VERY SOL IN WATER, ETHYL ALCOHOL, ACETONE; SPARINGLY SOL IN BENZENE. SMILES: CCOC(=O)C#C. InChI: InChI=1S/C5H6O2/c1-3-5(6)7-4-2/h1H,4H2,2H3. InChIKey: FMVJYQGSRWVMQV-UHFFFAOYSA-N. | |
Propargyl Benzyl Ether Quick inquiry Where to buy Suppliers range | A propargyl derivative used in the synthesis of substituted carbocyclic aromatic compounds and pharmaceutical compounds. Group: Biochemicals. Alternative Names: ( ( (Propargyl) oxy) methyl) benzene; 1- (Benzyloxymethyl) ethyne; 1-Benzyloxy-2-propyne; 2-Propynyl benzyl Ether; 3-(Benzyloxy)-1-propyne; 3-(Benzyloxy)propyne; Benzyl 2-propynyl Ether; Benzyl Propargyl Ether; O-Benzyl Propargyl Alcohol; [ (2-Propynyloxy) methyl]benzene. Grades: Highly Purified. CAS No. 4039-82-1. Pack Sizes: 500mg, 5g, 25g, 50g. US Biological Life Sciences. | Worldwide |
Propargyloxy-t-butyldimethylsilane Quick inquiry Where to buy Suppliers range | Transparent liquid. Group: Siloxanes. Alternative Names: t-butyldimethylsilyl propargyl ether; tert-butyldimethylpropargyloxysilane; TBDMS ether of propargyl alcohol; ghl.PD_Mitscher_leg0.449; UPCMLD00WV-88. Grades: 95%+. CAS No. 76782-82-6. Molecular formula: C9H18OSi. Mole weight: 170.32. IUPAC Name: tert-butyl-dimethyl-prop-2-ynoxysilane. Exact Mass: 170.11300. Boiling Point: 157.8ºC at 760 mmHg. Flash Point: 38.8ºC. Density: 0.838 g/cm3. SMILES: CC(C)(C)[Si](C)(C)OCC#C. InChIKey: ZYDKYFIXEYSNPO-UHFFFAOYSA-N. Safty Description: 16. | |
Propargyl Tosylate Quick inquiry Where to buy Suppliers range | Protected Propargyl. A possible genotoxic compound that can affect the bacterial and mammalian cell systems. Group: Biochemicals. Alternative Names: 2-Propyn-1-ol 4-Methyl Benzene sulfonate; 2-Propyn-1-ol p-Toluenesulfonate; 1-[(p-Toluenesulfonyl)oxy]-2-propyne; 2-Propynyl p-Toluenesulfonate; 2-Propynyl Tosylate; Propargyl Alcohol Tosylate; p-Toluenesulfonic Acid Propargyl Ester. Grades: Highly Purified. CAS No. 6165-76-0. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
(R)-(+)-BINAP Quick inquiry Where to buy Suppliers range | (R)-(+)-BINAP. Uses: (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. Ligand employed in rhodium-catalyzed 1,4-additions to enones. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. Ligand employed in palladium-catalyzed synthesis of chiral allenes. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organyl compounds to cyclic enones. Ligand employed in iridium-catalyzed transfer hydrogenative allylation of benzylic alcohols. Ligand employed in rhodium-catalyzed asymmetric C-Si bond formation by conjugate silyl transfer using a Si-B linkage. Ligand employed in the iridium-catalyzed asymmetric cyclopropane-mediated carbonyl allylation of primary alcohols. Ligand employed in the nickel-catalyzed asymmetric α-arylation of tetralones. Ligand employed in the copper-catalyzed asymmetric propargylation of ketones. Ligand employed in the cobalt-catalyzed asymmetric reductive coupling of alkynes with alkenes. Ligand employed in the rhodium-catalyzed asymmetric 1,4-addition of arylalanes on trisubstituted enones. Ruthenium-catalyzed asymmetric hydrocyanation of imines. Palladium-catalyzed asymmetric intermolecular cyclization. Group: Organic Phosphine Compounds. Alternative Names: -Bis(d | |
Silver methanesulfonate Quick inquiry Where to buy Suppliers range | Silver methanesulfonate. Uses: Gold Catalysts-21st Century'Gold Rush' Catalyst for:Heterocyclization reactions. CO2-mediated rearrangement of propargyl alcohols for the synthesis of a,?-unsaturated ketones and esters. Group: Silver series of catalysts. Alternative Names: MLKQJVFHEUORBO-UHFFFAOYSA-M; Silvermesylate; 2386-52-9; Methanesulfonic acid, silver(1+) salt (1:1); EINECS 219-199-2; SCHEMBL564771; NSC 83223; Silver(I) methanesulfonate; RT-000531; CTK3J2352. CAS No. 2386-52-9. Molecular formula: CH3AgO3S. Mole weight: 202.96g/mol. IUPAC Name: silver;methanesulfonate. Exact Mass: 201.885g/mol. EC Number: 219-199-2. SMILES: CS(=O)(=O)[O-].[Ag+]. InChI: InChI=1S/CH4O3S.Ag/c1-5(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1. InChIKey: MLKQJVFHEUORBO-UHFFFAOYSA-M. | |
Tetrahydro-2-(2-propynyloxy)-2H-pyran Quick inquiry Where to buy Suppliers range | Colorless liquid. Group: Heterocyclic Organic Compound. Alternative Names: 2-(2-PROPYNYLOXY)TETRAHYDROPYRAN; TETRAHYDRO-2-(2-PROPYNYLOXY)-2H-PYRAN; TIMTEC-BB SBB008982;PROPARGYL ALCOHOL TETRAHYDRO-2H-PYRAN ETHER;1-(2'-Tetrahydropyranyloxy)-2-propyne;2-(Propargyloxy)tetrahydropyran;2-Propargyloxane;2-Propynyl 2-pyranyl ether. Grades: >97.0%(GC). CAS No. 6089-4-9. Molecular formula: C8H12O2. Mole weight: 140.18. IUPAC Name: 2-prop-2-ynoxyoxane. Exact Mass: 140.08400. EC Number: 228-027-5. Boiling Point: 63-65ºC9 mm Hg(lit.). Flash Point: 139 °F. Density: 0.997. SMILES: C#CCOC1CCCCO1. InChIKey: HQAXHIGPGBPPFU-UHFFFAOYSA-N. H-Bond Donor: 0. H-Bond Acceptor: 2. Safty Description: S26-S27-S28-S36-S37-S39. Hazard statements: Xi. | |
Triethylene Glycol Mono(2-propynyl) Ether Quick inquiry Where to buy Suppliers range | Triethylene Glycol Mono(2-propynyl) Ether is a polyethylene glycol (PEG)-based PROTAC linker that can be used in the synthesis of a series of PROTACs. Synonyms: Propargyl-PEG4-alcohol; Propargyl-PEG3-alcohol; Alkyne-PEG3-OH; 2-(2-(2-(Prop-2-yn-1-yloxy)ethoxy)ethoxy)ethanol; 2-[2-[2-(2-Propynyloxy)ethoxy]ethoxy]ethanol; 2-{2-[2-(prop-2-yn-1-yloxy)ethoxy]ethoxy}ethan-1-ol; Triethylene Glycol Monopropargyl Ether; Ethanol, 2-[2-[2-(2-propynyloxy)ethoxy]ethoxy]-. Grades: >95%. CAS No. 208827-90-1. Molecular formula: C9H16O4. Mole weight: 188.22. | |
Tris (acetonitrile) cyclopentadienylruthenium (II) Hexafluorophosphate Quick inquiry Where to buy Suppliers range | yellow to orange powder. Uses: Catalyst used for the coupling of allene with activated olefines to form 1,3-diene. Catalyst used for the dimerization of propargyl alcohols. Catalyst used in the Trost's ruthenium-catalyzed ene-yne cross-coupling reaction. Catalyst for asymmetric cyclization of ω-hydroxy allyl alcohols to give α-alkenyl cyclic ethers. Catalyst for synthesis of furans from bis(alkynes) and DMSO. Group: Ruthenium series catalysts. Alternative Names: (Cyclopentadienyltris (acetonitrile)ruthenium hexafluorophosphate. Grades: 0.98. CAS No. 80049-61-2. Molecular formula: C11H14F6N3PRu. Mole weight: 434.29. Symbol: GHS07. Safty Description: Warning. Hazard statements: H315-H319-H335. | |
Tris(triphenylphosphine)rhodium(I) Chloride Quick inquiry Where to buy Suppliers range | Tris(triphenylphosphine)rhodium(I) Chloride. Uses: A homogeneous hydrogenation catalyst which operates under mild conditions. Catalyst for the decarbonylation of aldehydes. Catalyst for regio- and stereoselective allylic substitution reactions. Alkyne hydro-phosphorylation Heck-type reaction with α,β-unsaturated esters. Alkyne arylation Allylic alcohol-olefin coupling. Terminal alkenes from ketones. Rh-catalyzed isomerization of α-aryl propargyl alcohols to indanones. Reductive deprotection of silyl groups. Group: Rhodium series of catalysts. Alternative Names: Wilkinson's catalyst Tris(triphenylphosphine)rhodium(I) chloride C54H45ClP3Rh 925.23 ca 250 degrees dec. 14694-95-2 "14,10047" 238-744-5 MFCD00010016 P273-P501a; Tris(triphenylphosphine)rhodium chloride; AS-12487; AN-15374; Tris(triphenylphosphine)rhodium monochloride; 16592-65-7; RhCl(PPh3)3, Rhodium(I) tris(triphenylphosphine) chloride, Wilkinson's catalyst, NSC 124140; chlorotris(triphenylphosphine)-rhodium(i); RTR-005847; tris(triphenylphosphine)-rhodium (I) chloride. CAS No. 14694-95-2. Molecular formula: C54H45ClP3Rh-. Mole weight: 925.231g/mol. IUPAC Name: rhodium;triphenylphosphane;chloride. Rotatable Bond Count: 9. Exact Mass: 924.148g/mol. EC Number: 238-744-5. SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Cl-]. [Rh]. InChI: InChI=1S/3C18H15P.ClH.Rh/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;/h3*1-15H;1H;/p-1. InChIKey: QBERHIJABFXGRZ-UHFFFAOYSA-M. H-Bond Acceptor: 1. Monoisotopic Mass: 924.148g/mol. |