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| Product | Description | |
|---|---|---|
| Trifluoromethanesulfonic Acid, Anhydride | Trifluoromethanesulfonic Acid, Anhydride. CAS No. 358-23-6. Categories: trifluoromethanesulfonic anhydride. |  Pennsylvania PA |
| Trifluoromethanesulfonic acid silver | Trifluoromethanesulfonic acid (Triflic acid) silver, a perfluoroalkanesulfonic acid, is one of the superior catalysts for C- or O-acylation [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Triflic acid silver; Perfluoromethanesulfonic acid silver; Fluorad FC 24 silver. CAS No. 2923-28-6. Pack Sizes: 10 g; 25 g. Product ID: HY-W020983. |  |
| Trifluoromethanesulfonic acid sodium | Sodium trifluoromethanesulfonate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Triflic acid sodium; Perfluoromethanesulfonic acid sodium; Fluorad FC 24 sodium. CAS No. 2926-30-9. Pack Sizes: 5 g; 25 g. Product ID: HY-W016916. | |
| 1,2,3-trimethylimidazolium trifluoromethanesulfonate | Metal Plating, Electropolishing, Metal Reprocessing, Phase transfer media, Batteries Fuel Cells, Nanomaterials, Industrial Solvents, Nuclear Fuel Red Waste, Enzymatic Catalysis, Lubricants Heat Transfer and Solar Energy Conversion. Group: Heterocyclic organic compound. Alternative Names: 1,2,3-Trimethylimidazolium trifluoromethanesulfonate, Trifluoromethanesulfonic acid 1,2,3-Trimethylimidazolium salt, 05942_FLUKA, CTK8F2856, AG-L-62869, 439286-64-3. CAS No. 439286-64-3. Molecular formula: C7H11F3N2O3S. Mole weight: 260.23. Purity: 98% min. IUPACName: trifluoromethanesulfonate;1,2,3-trimethylimidazol-1-ium. Canonical SMILES: CC1=[N+](C=CN1C)C. C(F)(F)(F)S(=O)(=O)[O-]. Catalog: ACM439286643. |  |
| 2-Bromoethyl trifluoromethanesulphonate | 2-Bromoethyl trifluoromethanesulphonate. Alternative Names: 1,1,1-TrifluoroMethanesulfonic acid 2-broMo-ethyl ester. CAS No. 103935-47-3. Molecular formula: C3H4BrF3O3S. Mole weight: 257. Appearance: Liquid. Purity: 0.95. Catalog: ACM103935473. | |
| 3-(Aminocarbonyl)-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-pyridinium Triflate | 3-(Aminocarbonyl)-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-pyridinium Triflate is an intermediate in synthesizing β-Nicotinamide Mononucleotide, a product of the extracellular Nicotinamide phosphoribosyltransferase (eNAMPT) reaction and a key NAD+ intermediate. It ameliorates glucose intolerance by restoring NAD+ levels in HFD-induced T2D mice. It also enhances hepatic insulin sensitivity and restores gene expression related to oxidative stress, inflammatory response, and circadian rhythm, partly through SIRT1 activation. Synonyms: 3-(Aminocarbonyl)-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-pyridinium 1,1,1-Trifluoromethanesulfonate; 3-(Aminocarbonyl)-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-pyridinium Salt with Trifluoromethanesulfonic Acid. CAS No. 774599-53-0. Molecular formula: C17H21N2O8? CF3O3S?. Mole weight: 381.36. |  |
| Chloromethyl Polystyrene | The Merrifield resin has in the past been the standard support for the synthesis of peptide acids by Boc strategy. Originally, the cesium salt of a protected amino acid was anchored to the chloromethyl support via nucleophilic displacement of chlorine. Although, Me4N salts, sodium salts in THF with Bu4NF catalysis and more recently zinc salts in EtOH have also been used. Cleavage is normally effected by treatment with HF or trifluoromethanesulfonic acid or by hydrogenolysis, alcohols can be released by using diisobutylaluminium hydride or LiBH4. For cleavage scavengers may be required. Uses: New isomeric trialkoxybenzylamine resins have been developed by coupling phthalimidomethyl-3,5-dimethoxyphenols to this resin followed by subsequent treatment with hydrazine, which allows dcc coupling with the carboxyl function of amino acids or peptides. the addition of alcohols can be performed by heating the corresponding potassium or sodium alkoxide and the resin in dmf. reductive cleavage of. Group: Merrifield resins. Alternative Names: Merrifield Resin. CAS No. 55844-94-5. Pack Sizes: 25g, 100g. |  |
| Cyclic-Oligo Bis[(1R,2R)-(+)-1,2-cyclohexanediamino-N,N-bis(3,3-di-t-butylsalicylidene) cobalt(III)triflate]-5,5-bis(2-carboxyethyl)ether | Oligomeric catalyst used for the hydrolytic kinetic resolution of terminal epoxides under solvent-free conditions. Oligomeric catalyst used for the synthesis of highly enantioenriched trans-1,2-amino alcohols. Group: Cobalt catalysts. Alternative Names: MFCD28144555;647036-07-5;Cyc.-Oligo Bis[(1R,2R)-1,2-cyclohexanediamino-N,N'-bis(3,3'-di-t-butylsalicylidene) Co(III)OTf]-5,5'-bis(2-carboxyethyl)ether. CAS No. 647036-07-5. Molecular formula: C70H90Co2F6N4O20S2. Mole weight: 1603.475g/mol. IUPACName: cobalt;(4R, 9R, 33R, 38R)-14, 28, 43, 57-tetratert-butyl-13, 29, 42, 58-tetrahydroxy-17, 21, 25, 46, 50, 54-hexaoxa-3, 10, 32, 39-tetrazaheptacyclo[53.3.1.112, 16.126, 30.141, 45.04, 9.033, 38]dohexaconta-1(58), 2, 10, 12, 14, 16(62), 26(61), 27, 29, 31, 39, 41, 43, 45(60), 55(59), 56-hexadecaene-18, 24, 47, 53-tetrone;trifluoromethanesulfonic acid. Canonical SMILES: CC (C) (C)C1=C (C2=CC (=C1)OC (=O)CCOCCC (=O)OC3=CC (=C (C (=C3)C=NC4CCCCC4N=CC5=CC (=CC (=C5O)C (C) (C)C)OC (=O)CCOCCC (=O)OC6=CC (=C (C (=C6)C=NC7CCCCC7N=C2)O)C (C) (C)C)O)C (C) (C)C)O. C (F) (F) (F)S (=O) (=O)O. C (F) (F) (F)S (=O) (=O)O. [Co]. [Co]. Catalog: ACM647036075. | |
| Cyclic-Oligo Bis[(1S,2S)-(-)-1,2-cyclohexanediamino-N,N-bis(3,3-di-t-butylsalicylidene) cobalt(III)triflate]-5,5-bis(2-carboxyethyl)ether | Oligomeric catalyst used for the hydrolytic kinetic resolution of terminal epoxides under solvent-free conditions. Catalyst used for the synthesis of enantioenriched tetrahydrofurans via the intramolecular openings of oxetanes. Catalyst for the enantioselective addition of phenyl carbamate to meso-epoxides for the synthesis of trans-1,2-amino alcohols. Group: Cobalt catalysts. Alternative Names: MFCD28144556;1252661-94-1;Cyc-Oligo Bis[(1S,2S)-(-)-1,2-cyclohexanediamino-N,N'-bis(3,3'-di-t-Busalicylidene) Co(III)OTf]-5,5'-bis(2-carboxyEt)ether;Cyclic-Oligo Bis[(1S,2S)-(-)-1,2-cyclohexanediamino-N,N'-bis(3,3'-di-t-butylsalicylidene) cobalt(III)triflate]-5,5'-bis(2-carboxyethyl)ether. CAS No. 1252661-94-1. Molecular formula: C70H90Co2F6N4O20S2. Mole weight: 1603.475g/mol. IUPACName: cobalt;(4S, 9S, 33S, 38S)-14, 28, 43, 57-tetratert-butyl-13, 29, 42, 58-tetrahydroxy-17, 21, 25, 46, 50, 54-hexaoxa-3, 10, 32, 39-tetrazaheptacyclo[53.3.1.112, 16.126, 30.141, 45.04, 9.033, 38]dohexaconta-1(58), 2, 10, 12, 14, 16(62), 26(61), 27, 29, 31, 39, 41, 43, 45(60), 55(59), 56-hexadecaene-18, 24, 47, 53-tetrone;trifluoromethanesulfonic acid. Canonical SMILES: CC (C) (C)C1=C (C2=CC (=C1)OC (=O)CCOCCC (=O)OC3=CC (=C (C (=C3)C=NC4CCCCC4N=CC5=CC (=CC (=C5O)C (C) (C)C)OC (=O)CCOCCC (=O)OC6=CC (=C (C (=C6)C=NC7CCCCC7N=C2)O)C | |
| Ethyl trifluoromethanesulfonate | Ethyl trifluoromethanesulfonate. Group: other electronic materials. Alternative Names: Ethyl Triflate; Ethyl trifluoromethanesulphonate; Trifluoromethanesulfonic Acid Ethyl Ester; Trifluoromethanesulfonic acid ethyl ester; ethyltrifluoromethane sulfonate; ethyltriflate. CAS No. 425-75-2. Product ID: ethyltrifluoromethanesulfonate. Molecular formula: 178.12. Mole weight: C3< / sub>H5< / sub>F3< / sub>O3< / sub>S. CCOS(=O)(=O)C(F)(F)F. UVECLJDRPFNRRQ-UHFFFAOYSA-N. 98%. | |
| Methanesulfonic acid,1,1,1-trifluoro-,3-pyridinyl ester | Heterocyclic Organic Compound. Alternative Names: 3-Pyridyl Trifluoromethanesulfonate, 3-Pyridyl Triflate, 107658-27-5, AG-D-23409, ACMC-1BO5L, CTK4A5575, 3-Trifluoromethanesulfonyloxypyridine, ANW-15836, AKOS015910975, FT-0674235, P1860, PYRIDIN-3-YL TRIFLUOROMETHANESULFONATE, Trifluoromethanesulfonic Acid 3-Pyridyl Ester, I14-38435, 1,1,1-Trifluoro-methanesulfonic Acid 3-Pyridinyl Ester, Methanesulfonic acid,1,1,1-trifluoro-, 3-pyridinyl ester, Methanesulfonicacid, trifluoro-, 3-pyridinyl ester (9CI); 3-Pyridinyl triflate; 3-Pyridyltriflate; 3-Pyridyl trifluoromethanesulfonate;3-Trifluoromethanesulfonyloxypyridine. CAS No. 107658-27-5. Molecular formula: C6H4F3NO3S. Mole weight: 227.1610696. Purity: 0.96. IUPACName: pyridin-3-yl trifluoromethanesulfonate. Canonical SMILES: C1=CC(=CN=C1)OS(=O)(=O)C(F)(F)F. Catalog: ACM107658275. | |
| Methyl trifluoromethanesulfonate | Methyl trifluoromethanesulfonate. Group: other electronic materials. Alternative Names: methyl-triflate; EINECS 206-371-7; Trifluoromethanesulfonic Acid Methyl Ester; Methyltrifluoromethanesulfonate; Methyl Trifluoromethanesulfonate; trifluoromethanesulphonic acid methyl ester; Methyl triflate; Methanesulfonic acid,trifluoro-,methyl ester; Methyl trifluoromethane sulfonate; Methyl trifluoromethanesulphonate. CAS No. 333-27-7. Product ID: methyltrifluoromethanesulfonate. Molecular formula: 164.1. Mole weight: C2< / sub>H3< / sub>F3< / sub>O3< / sub>S. COS(=O)(=O)C(F)(F)F. OIRDBPQYVWXNSJ-UHFFFAOYSA-N. 97%. | |
| Nicotinamide Riboside Triflate (α/β mixture) | Nicotinamide analog, Nicotinamide riboside (β-NAR) is an intermediate in one biosynthetic pathway by which Nicotamide is converted into NAD (Nicotinamide Adenine Dinucleotide). Uses: Nicotinamide analog. nicotinamide riboside (β-nar) is an intermediate in one biosynthetic pathway by which nicotamide is converted into nad (nicotinamide adenine dinucleotide) cas 1341-23-7 for free base form. Synonyms: 3-(Aminocarbonyl)-1-D-ribofuranosylpyridinium Trifluoromethanesulfonic Acid Salt;Nicotinamide Ribose Triflate; Nicotinamide Ribonucleoside Triflate; NAR; Ribosylnicotinamide Triflate. Grades: 97%. CAS No. 445489-49-6. Molecular formula: C12H15F3N2O8S. Mole weight: 404.32. | |
| (S)-(+)-1,1'-Binaphthyl-2,2'-diyl Bis(trifluoromethanesulfonate) | Heterocyclic Organic Compound. Alternative Names: TRA0083230; KS-00000Z2O; (R)-BINOL-TF2; (aS)-1, 1'-Binaphthalene-2, 2'-diyl=bis (trifluoromethanesulfonate); (aR)-2, 2'-Bis(trifluoromethylsulfonyloxy)-1, 1'-binaphthalene; S-1,1'-BINAPHTHOL-2,2'-BIS(TRIFLUOROMETHANESULFONATE); TRIFLUOROMETHANESULFONIC ACID 2'-TRIFLUOROMETHANESULFONYLOXY-[1, 1']BINAPHTHALENYL-2-YL ESTER; TL8000668; 1,1'-binaphthalen-2,2'-diylbis(trifluormethansulfonat); AC-8072. CAS No. 128544-05-8. Molecular formula: C22H12F6O6S2. Mole weight: 550.442g/mol. IUPACName: [1-[2- (trifluoromethylsulfonyloxy) naphthalen-1-yl]naphthalen-2-yl] trifluoromethanesulfonate. Canonical SMILES: C1=CC=C2C (=C1)C=CC (=C2C3=C (C=CC4=CC=CC=C43)OS (=O) (=O)C (F) (F)F)OS (=O) (=O)C (F) (F)F. ECNumber: 603-149-5. Catalog: ACM128544058. | |
| Scandium(III) triflate | Water tolerant Lewis acid. Commonly used in a range of Lewis acid catalyzed reactions. Efficient metal source for Lewis acid catalyzed asymmetric reactions. Catalyzes Friedel-Crafts alkylation, acylation and related reactions. Catalyzes various domino- and multi-component processes. Catalyzes electrophilic additions of alpha-diazoesters with ketones. Catalyzes carbon insertion reactions. Group: Scandium catalysts. Alternative Names: Scandium(III) trifluoromethanesulfonate; KSC174E3P; KS-000002BK; Trifluoromethanesulfonic acid scandium(III) salt; ACT08645; RTR-005607; SCANDIUM TRIS(TRIFLUOROMETHANESULFONATE); SC(SO3CF3)3; scandium(3+); scandium (III)trifluoromethanesulfonate. CAS No. 144026-79-9. Molecular formula: C3F9O9S3Sc. Mole weight: 492.16 g/mol. IUPACName: scandium(3+); trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Sc+3]. Catalog: ACM144026799. | |
| Silver(?) trifluorometanesulfonate | Synonyms: AgOTf; CF3SO3Ag; Trifluoromethanesulfonic acid silver salt; Silver triflate; Silver(?) triflate. Grades: >98.0%(T). CAS No. 2923-28-6. Molecular formula: CF3SO3Ag. Mole weight: 256.94. | |
| Tetrabutylammonium Trifluoromethanesulfonate | Tetrabutylammonium Trifluoromethanesulfonate. Group: Battery materials electronic materials. Alternative Names: Tetrabutylammonium Triflate Trifluoromethanesulfonic Acid Tetrabutylammonium Salt. CAS No. 35895-70-6. Product ID: tetrabutylazanium; trifluoromethanesulfonate. Molecular formula: 391.53. Mole weight: C17H36F3NO3S. CCCC[N+](CCCC)(CCCC)CCCC. C(F)(F)(F)S(=O)(=O)[O-]. 1S/C16H36N. CHF3O3S/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; 2-1(3, 4)8(5, 6)7/h5-16H2, 1-4H3; (H, 5, 6, 7)/q+1; /p-1. YNJQKNVVBBIPBA-UHFFFAOYSA-M. >98.0%(T). | |
| Tetrakis(acetonitrile) trifluoromethanesulfonate Copper | . Uses: Transition metal catalysts. Synonyms: Tetrakis (acetonitrile)copper (I)Trifluoromethanesulfonate; Copper(1+), tetrakis(acetonitrile)-, (T-4)-, 1,1,1-trifluoromethanesulfonate (1:1); Copper(1+), tetrakis(acetonitrile)-, (T-4)-, salt with trifluoromethanesulfonic acid (1:1); Methanesulfonic acid, trifluoro-, ion(1-), (T-4)-tetrakis(acetonitrile)copper(1+); Tetrakis(acetonitrile)copper triflate; Tetrakis(acetonitrile)copper trifluoromethanesulfonate; Tetrakis(acetonitrile)copper(1+) triflate; Tetrakis(acetonitrile)copper(1+) triflate(1-); Tetrakis(acetonitrile)copper(1+) trifluoromethanesulfonate; Tetrakis(acetonitrile)copper(1+) trifluoromethanesulfonate(1-); Tetrakis(acetonitrile)copper(I) triflate; Tetrakis(acetonitrile)copper(I) trifluoromethanesulfonate. Grades: ≥95%. CAS No. 58452-28-1. Molecular formula: C8H12CuN4.CF3O3S. Mole weight: 376.82. | |
| Tetrakis(pyridine)copper(II) triflate | Heterocyclic Organic Compound. Alternative Names: Cu(pyridine)4(OTf)2, Tetrakis(pyridine)copper(II) triflate, Tetrakis(pyridine)copper(II) bis(trifluoromethanesulfonate), 113110-58-0. CAS No. 113110-58-0. Molecular formula: C22H22CuF6N4O6S2. Mole weight: 678.08. Purity: 0.96. IUPACName: copper; pyridine; trifluoromethanesulfonic acid. Canonical SMILES: C1=CC=NC=C1. C1=CC=NC=C1. C1=CC=NC=C1. C1=CC=NC=C1. C(F)(F)(F)S(=O)(=O)O. C(F)(F)(F)S(=O)(=O)O. [Cu]. Catalog: ACM113110580. | |
| Triflic acid | Triflic acid. CAS No. 1493-13-6. Categories: trifluoromethanesulfonic acid. | Pennsylvania PA |
| Trifluoro-methanesulfonic acid 2-methoxy-4-formyl-6-nitro-phenyl ester | Heterocyclic Organic Compound. Alternative Names: 1021493-52-6, CTK4A0738, AG-L-60538, AK137405, KB-62061, 4-Formyl-2-methoxy-6-nitrophenyl trifluoromethanesulfonate, Trifluoromethanesulfonic acid 2-methoxy-4-formyl-6-nitrophenyl ester, Trifluoro-methanesulfonic acid 2-methoxy-4-formyl-6-nitro-phenyl ester. CAS No. 1021493-52-6. Molecular formula: C9H6F3NO7S. Mole weight: 329.206650 [g/mol]. Purity: 0.96. IUPACName: (4-formyl-2-methoxy-6-nitrophenyl) trifluoromethanesulfonate. Canonical SMILES: COC1=CC (=CC (=C1OS (=O) (=O)C (F) (F)F)[N+] (=O)[O-])C=O. Catalog: ACM1021493526. | |
| Trimethylsilyl trifluoromethanesulfonate | Trimethylsilyl trifluoromethanesulfonate. Group: other electronic materials. Alternative Names: TMS triflate, TMSOTf, Trifluoromethanesulfonic acid trimethylsilylester. CAS No. 27607-77-8. Pack Sizes: 10 g; 100 g. Product ID: tri methyl silyltrifluoromethanesulfonate. Molecular formula: 222.26. Mole weight: C4H9F3O3SSi. C[Si](C)(C)OS(=O)(=O)C(F)(F)F. FTVLMFQEYACZNP-UHFFFAOYSA-N. 99%. | |
| Zinc trifluoromethanesulfonate | Catalyst for the addition of acetylenes to carbonyls and nitrones. Claisen rearrangement. Catalyst for the enantioselective Henry and Aza-Henry reactions. Pd-catalyzed hydroalkylation of styrenes with zinc reagents. Group: Zinc catalysts. Alternative Names: 2CHF3O3S.Zn; AK158308; SCHEMBL165265; zinc tris(fluoranyl)methanesulfonate; DB-009916; AB1011131; Zinc(II) Triflate; AKOS005258662; Trifluoromethanesulfonic acid zinc salt; RTR-019094. CAS No. 54010-75-2. Molecular formula: C2F6O6S2Zn. Mole weight: 363.506g/mol. IUPACName: zinc;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Zn+2]. ECNumber: 258-922-6. Catalog: ACM54010752. | |
| 1-butylsulfonic-3-methylimidazolium trifluoromethanesulfonate | Metal Plating, Electropolishing, Metal Reprocessing, Phase transfer media, Batteries Fuel Cells, Nanomaterials, Industrial Solvents, Nuclear Fuel Red Waste, Enzymatic Catalysis, Lubricants Heat Transfer and Solar Energy Conversion. Group: Other ionic liquidssulfonic acid functionalized ionic liquidsother imidazolium-based ionic liquids. CAS No. 57414-80-7. Molecular formula: C9H15F3N2O6S2. Mole weight: 368.3504. Purity: 98% min. Catalog: ACM57414807. | |
| 1-Methyl-3-(4-sulfobutyl)imidazolium Bis(trifluoromethanesulfonyl)imide | 1-Methyl-3-(4-sulfobutyl)imidazolium Bis(trifluoromethanesulfonyl)imide. Group: Battery materials. CAS No. 909390-59-6. Product ID: bis(trifluoromethylsulfonyl)azanide; 4-(3-methylimidazol-3-ium-1-yl)butane-1-sulfonic acid. Molecular formula: 499.41. Mole weight: C10H15F6N3O7S3. C[N+]1=CN (C=C1)CCCCS (=O) (=O)O. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. 1S/C8H14N2O3S. C2F6NO4S2/c1-9-5-6-10 (8-9)4-2-3-7-14 (11, 12)13; 3-1 (4, 5)14 (10, 11)9-15 (12, 13)2 (6, 7)8/h5-6, 8H, 2-4, 7H2, 1H3; /q; -1/p+1. PXYKADKIWNXJNF-UHFFFAOYSA-O. >95.0%(T). | |
| 2-(2,3-Naphthalimino)ethyl trifluoromethanesulfonate | Heterocyclic Organic Compound. Alternative Names: METHANESULFONIC ACID, TRIFLUORO-2-(1,3-DIHYDRO-1,3-DIOXO-2H-BENZ[F]ISO-INDOL-2-YL)ETHYL ESTER;2-(2,3-NAPHTHALIMINO)ETHYL TRIFLUOROMETHANESULFONATE;2-(2 3-NAPHTHALIMINO)ETHYL TRIFLUOROMETH. CAS No. 128651-50-3. Molecular formula: C15H10F3NO5S. Mole weight: 345.34. Catalog: ACM128651503. | |
| 2-Methyl-5-pyridinetrifluoromethanesulf& | Heterocyclic Organic Compound. Alternative Names: 2-Methyl-5-pyridyl triflate, 2-Methyl-5-pyridinetrifluoromethanesulfonate, AGN-PC-001RKE, 648485_ALDRICH, I14-105492, Methanesulfonic acid, trifluoro-, 6-methyl-3-pyridinyl ester, 111770-91-3. CAS No. 111770-91-3. Molecular formula: C7H6F3NO3S. Mole weight: 241.19. Purity: 0.96. IUPACName: (6-methylpyridin-3-yl) trifluoromethanesulfonate. Canonical SMILES: CC1=NC=C(C=C1)OS(=O)(=O)C(F)(F)F. Density: 1.412 g/mL at 25ºC(lit.). Catalog: ACM111770913. | |
| 4-(3-Butyl-1-imidazolio)-1-butanesulfonic acid triflate | 4-(3-Butyl-1-imidazolio)-1-butanesulfonic acid triflate is a Bronsted acidic ionic liquid. Group: Heterocyclic organic compound. Alternative Names: 1-Butyl-3-(4-sulfobutyl)imidazolium triflate. CAS No. 439937-63-0. Molecular formula: C12H21F3N2O6S2. Mole weight: 410.43. Appearance: Liquid. Purity: 0.96. IUPACName: 4-(3-butylimidazol-1-ium-1-yl)butane-1-sulfonic acid;trifluoromethanesulfonate. Canonical SMILES: CCCCN1C=C[N+](=C1)CCCCS(=O)(=O)O. C(F)(F)(F)S(=O)(=O)[O-]. Catalog: ACM439937630. | |
| 7-Coumaryl triflate | Heterocyclic Organic Compound. Alternative Names: 1,1,1-Trifluoro-methanesulfonic Acid 2-Oxo-2H-1-benzopyran-7-yl Ester. CAS No. 108530-10-5. Molecular formula: C10H5F3O5S. Mole weight: 294.2. Appearance: Yellow Solid. Purity: 0.96. IUPACName: (2-oxochromen-7-yl) trifluoromethanesulfonate. Catalog: ACM108530105. | |
| Aluminum trifluoromethanesulfonate | Friedel-Crafts Reactions. Aluminum trifluoromethanesulfonate has been used for the Friedel-Crafts alkylation reaction of toluene with isopropyl and tert-butyl chlorides (eq 1), and for theacylationof Benzene andtoluenewithacetylandbenzoylchlo- rides in low to moderate yields. Intramolecular Friedel-Crafts acylation of an aromatic compound with Meldrum's acid has also been reported using catalytic amounts of Al(OTf) 3. Acylation of 2-methoxynaphthalene with acetic anhydride has been reported using Al(OTf) 3 and lithium perchlorate as an additive to afford the corresponding 6-acetylated adduct in 83% yield. Effective acylation of arenes with carboxylic acids has also been disclosed using polystyrene-supported Al(OTf)3. Group: Organic aluminium. Alternative Names: Aluminum triflate. CAS No. 74974-61-1. Molecular formula: C3AlF9O9S3. Mole weight: 474.2. Appearance: Powder. Purity: 0.99. IUPACName: aluminum;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Al+3]. Catalog: ACM74974611-1. | |
| Bismuth(III) trifluoromethanesulfonate | Catalyst for organic syntheses. Group: Heterocyclic organic compound. Alternative Names: Methanesulfonic acid, 1,1,1-trifluoro-, bismuth(3+) salt (3:1). CAS No. 88189-03-1. Molecular formula: C3BiF9O9S3. Mole weight: 656.2. Appearance: Liquid. Purity: 0.99. IUPACName: bismuth;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Bi+3]. Catalog: ACM88189031-1. | |
| Cerium Chloride Anhydrous | Cerium Chloride, in forms of crystalline aggregates or lHight yellow lump aggregates, is the important material for catalyst, glass, phosphors and polishing powders. It is also used to decolorize glass by keeping iron in its ferrous state. The ability of Cerium-doped glass to block out ultra violet lHight is utilized in the manufacturing of medical glassware and aerospace windows. It is also used to prevent polymers from darkening in sunlHight and to suppress discoloration of television glass. It is applied to optical components to improve performance. Uses: Used as petroleum catalyst, automobile exhaust catalysts, organic synthesis catalyst, pharmaceutical intermediates, also used as a starting point for the preparation of other cerium salts, such as the lewis acid, cerium(iII) trifluoromethanesulfonate, used for friedel-crafts acylations. it can be used itself as a lewis acid, for example as a catalyst in friedel-crafts alkylation reactions. Group: Ce. CAS No. 779008-60-5. Molecular formula: CeCl3. Mole weight: 246g/mol. Appearance: White crystalline. Density: 3.92g/mL. Catalog: ACM779008605. | |
| Copper(II) trifluoromethanesulfonate | Ring-Opening of epoxides and aziridines. Asymmetric conjugate addition of organozinc reagents to α,β-unsaturated ketones. Electrophilic addition of olefins. Asymmetric aziridination of olefins. Asymmetric cycloadditions and aldol condensations. Asymmetric Kharasch oxidation. Asymmetric Michael addition of enamides. Asymmetric O-H or O-R insertion reactions. Enantioselective intramolecular aminooxygenation of alkenes. Enantioselective addition of dialkylzinc reagents to N-acylpyridinium salts. Pd-catalyzed C-H functionalizations of oximes with arylboronic acids. Used as a Lewis acid in the Nazarov cyclization. Catalyst in the diacetoxylation olefins. Catalyst in the meta-selective direct arylation of α-aryl carbonyl compounds. Catalyst in the three-component coupling of amines, aldehydes, and alkynes. Group: Organic copper. Alternative Names: Copper(II) triflate. CAS No. 34946-82-2. Molecular formula: C2CuF6O6S2. Mole weight: 361.7. Appearance: Powder. Purity: 99%+. IUPACName: copper;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Cu+2]. ECNumber: 252-300-8. Catalog: ACM34946822-1. | |
| Methanesulfonic Acid, 1,1,1-Trifluoro-, 6-[(1-Methylethyl)Thio]-1,3-Dioxo-1H-Benz[De]Isoquinolin-2(3H)-Yl Ester | Light-yellow powder; Strong acid (triflic acid) generation. Group: Photoacid generators. Alternative Names: 6-[(1-Methylethyl)Thio]-1,3-Dioxo-1H-Benz[De]Isoquinolin-2(3H)-Yl 1,1,1-Trifluoromethanesulfonate. CAS No. 1887001-94-6. Molecular formula: C16H12F3NO5S2. Mole weight: 419.4. Catalog: PR1887001946. | |
| Methanesulfonic Acid, 1,1,1-Trifluoro-, 6-(1-Octyn-1-Yl)-1,3-Dioxo-1H-Benz[De]Isoquinolin-2-Yl Ester | Light-yellow powder; Strong acid (triflic acid) generation. Group: Photoacid generators. Alternative Names: 6-(Oct-1-Yn-1-Yl)-1,3-Dioxo-1H-Benzo[De]Isoquinolin-2(3H)-Yl Trifluoromethanesulfonate. CAS No. 2004734-99-8. Molecular formula: C21H18F3NO5S. Mole weight: 453.43. Catalog: PR2004734998. | |
| Methanesulfonic acid,1,1,1-trifluoro-,cerium(4+)salt(4:1) | Heterocyclic Organic Compound. Alternative Names: cerium(4+), trifluoromethanesulfonate; Cerium(IV) trifluoromethanesulfonate. CAS No. 107792-63-2. Molecular formula: (CF3SO3)4Ce. Mole weight: 736.39. Appearance: Yellow powder. Purity: 0.96. IUPACName: cerium(4+);trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Ce+4]. Catalog: ACM107792632. | |
| N-Hydroxynaphthalimide triflate99+% | N-Hydroxynaphthalimide triflate99+%. Group: Self assembly and lithography. Alternative Names: N-HYDROXYNAPHTHALIMIDE TRIFLATE99+%; N-HYDROXYNAPHTHALIMIDE TRIFLATE, 99+%, E; Methanesulfonic acid, 1,1,1-trifluoro-, 1,3-dioxo-1H-benz[de]isoquinolin-2(3H)-yl ester; 1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl trifluoroMethanesulfonate; NHN-TF; N-Hydroxynapht. CAS No. 85342-62-7. Product ID: (1,3-dioxobenzo[de]isoquinolin-2-yl) trifluoromethanesulfonate. Molecular formula: 345.25g/mol. Mole weight: C13H6F3NO5S. C1=CC2=C3C (=C1)C (=O)N (C (=O)C3=CC=C2)OS (=O) (=O)C (F) (F)F. InChI=1S/C13H6F3NO5S/c14-13 (15, 16)23 (20, 21)22-17-11 (18)8-5-1-3-7-4-2-6-9 (10 (7)8)12 (17)19/h1-6H. LWHOMMCIJIJIGV-UHFFFAOYSA-N. | |
| Potassium trifluoromethanesulfonate, 99% | Potassium trifluoromethanesulfonate is used in studies of mixed alkali effects and short range interactions in poly(ethylene oxide) electrolytes,1 and characteristics of the electrochemical behavior of glassy carbon in super-acid media. Group: Heterocyclic organic compound. Alternative Names: J-017457; A819848; SBB090724; CF3SO3K; RL03005; Potassium trifluoromethanesulfonate, 98%; MFCD00042370; 2926-27-4; potassium,trifluoromethanesulfonate; Methanesulfonic acid, 1,1,1-trifluoro-, potassium salt (1:1). CAS No. 2926-27-4. Molecular formula: CF3KO3S. Mole weight: 188.162g/mol. IUPACName: potassium;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-].[K+]. ECNumber: 608-334-4. Catalog: ACM2926274. | |
| (R)-(-)-1,1'-Binaphthyl-2,2'-diyl Bis(trifluoromethanesulfonate) | Heterocyclic Organic Compound. Alternative Names: (R)-(-)-1,1''-Bi-2-naphthol bis(trifluoromethanesulfonate); 1,1'-Bi-2-naphthol bis(trifluoromethanesulfonate), 97%; A116079; (S)-(+)-BINOL-TF2; DTXSID10155257; (R)-(-)-1,1'-BIS(2-NAPHTHOL) DITRIFLATE; Methanesulfonic acid, 1, 1, 1-trifluoro-, 1, 1'-[1, 1'-binaphthalene]-2, 2'-diyl ester; (R)-(-)-1,1'-Binaphthyl-2,2'-diyl Bis(trifluoromethanesulfonate); (R)-(-)-1,1'-BI-2-NAPHTHYL BIS(TRIFLUOROMETHANESULFONATE); (R)-(-)-1,1'-BI-2-NAPHTHOL BIS(TRIFLUOROMETHANESUL. CAS No. 126613-06-7. Molecular formula: C22H12F6O6S2. Mole weight: 550.442g/mol. IUPACName: [1-[2- (trifluoromethylsulfonyloxy) naphthalen-1-yl]naphthalen-2-yl] trifluoromethanesulfonate. Canonical SMILES: C1=CC=C2C (=C1)C=CC (=C2C3=C (C=CC4=CC=CC=C43)OS (=O) (=O)C (F) (F)F)OS (=O) (=O)C (F) (F)F. ECNumber: 603-149-5. Catalog: ACM126613067. | |
| Silver trifluoromethanesulfonate | Silver precatalyst for the asymmetric allylation of aldehydes Silver catalyst for intramolecular additions of alcohols and carboxylic acids to inert olefins Silver catalyst for the fluorination of boronic acids Silver catalyst for the fluorination of functionalized aryl stannanes Silver catalyst for cyclopropenation of internal alkynes with donor/acceptor substituted diazo compounds Silver catalyst for the reaction of 2-alkynylbenzaldehyde with 2-isocyanoacetate. Group: Silver series of catalysts. Alternative Names: KSC491Q9D; Silver trifluoromethanesulfonate, >=99%; silver(1+) ion trifluoromethanesulfonate; silver(I)trifluoromethanesulfonate; TRIFLUOROMETHANESULFONATE SILVER SALT; trifluormethanesulfonic acid silver salt; silver(I) trifluoromethanesulphonate; ANW-26574; QRUBYZBWAOOHSV-UHFFFAOYSA-M; X7226. CAS No. 2923-28-6. Molecular formula: CAgF3O3S. Mole weight: 256.94. Appearance: Powder. Purity: 0.98. IUPACName: silver;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-].[Ag+]. ECNumber: 220-882-2. Catalog: ACM2923286-1. | |
| Tetrabutylammonium trifluoromethanesulfonate | Tetrabutylammonium trifluoromethanesulfonate, commonly known as TBAOTf. TBAOTf is widely used as a strong acid catalyst and phase transfer agent in organic synthesis, especially for reactions involving nucleophilic substitution, elimination, and rearrangement, in addition, it is also used as an electrolyte additive for rechargeable batteries and a stabilizer of supercritical fluids Due to its high stability, solubility and selectivity, TBAOTf is considered to be a highly efficient and multifunctional reagent in various applications. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 35895-70-6. Pack Sizes: 5 g; 10 g. Product ID: HY-W042557. | |
| Trifluoromethanesulfonate lithium | Trifluoromethanesulfonate (lithium) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Triflate lithium; Trifluoromethylsulfonate lithium; Trifluoromethanesulphonic acid lithium. CAS No. 33454-82-9. Pack Sizes: 25 g. Product ID: HY-21170B. | |
| Triphenylphosphinegold(I) bis (trifluoromethanesulfonyl)imidate, min. 98% | Catalyst promoting the addition of nucleophiles to alleneamides. Gold- and Bronsted acid-catalyzed cycloisomerization of 1,8-diynyl vinyl acetates to bicycle[2.2.1]hept-2-en-7-ones. Catalyst used for the synthesis of spiro[piperidine-3,3'-oxindoles]. Catalyst used in the gold(I)-catalyzed Rautenstrauch rearrangement. Gold-catalyzed π-directed regioselective cyclization of bis(o-alkynyl benzyl alcohols): rapid excess to dihydroisobenzofuran derivatives. Gold compound used in acid-catalyzed cycloisomerization - synthesis of diverse nitrogen-containing spiro heterocycles. Gold catalyst used in the domino synthesis of functionalized benzofurans and tetracyclic isochromans via formal carboalkoxylation. Group: Gold series of catalysts. CAS No. 866395-16-6. Molecular formula: C20H15AuF6NO4PS2. Mole weight: 739.4. Appearance: white to off-white powder. Purity: 0.99. Catalog: ACM866395166. | |
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