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产品详情
产品名称 英文名称:Hoveyda-Grubbs Catalyst 2nd Generation 同义词 (1,3-Bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(o-isopropoxyphenylmethylene)ruthenium 、 Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II)、Umicore Hoveyda-Grubbs Catalyst M720 、 Grubbs 催化剂® C627 产品性质 CAS编号:301224-40-8 分子式:C31H38Cl2N2ORu 分子量:626.62 MDL号:MFCD03701614 PubChem编号:11763533 别名:Umicore Hoveyda-Grubbs Catalyst M720 | Grubbs 催化剂® C627 英文别名:(1,3-Bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(o-isopropoxyphenylmethylene)ruthenium | Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II) 规格或纯度:≥97% 英文名称:Hoveyda-Grubbs Catalyst 2nd Generation 储存温度:2-8°C储存,充氩 运输条件:冰袋运输 产品介绍:Metathesis Ruthenium-Based Metathesis Catalysts Metathesis catalyst with efficiencies similar to Grubbs Catalyst 2nd generation but with different substrate specificity. Catalyzes ring-closing, ring-opening, and cross-metathesis reactions of highly electron-deficient substrates. Hoveyda-Grubbs 2nd Generation Catalyst &bull Phosphine free version of Grubbs 2nd Generation Catalyst with comparable reactivity, but initiates more readily at lower temperatures. &bull Efficient for metathesis of electron deficient substrates. &bull Catalyst for olefin cross metathesis with fluorinated olefins(CM) &bull Catalyst for ring closing metathesis(RCM)Product classCarbene Ligands, M-C, Homogeneous Catalysts, Grubbs Catalyst® 2nd Generation, Alkoxybenzylidene LigandsReaction typeAlkene Metathesis, Acyclic Diene Metathesis, Cross Metathesis, Ring Arrangement Metathesis , Ring Closing Metathesis, Ring Opening Metathesis Polymerization, Self MetathesisChemical propertiesChemical formulaC31H38Cl2N2ORuEmpirical formulaMolecular weight626.62MetalRuTheoretical metal content16Physical statepowderColorgreenApplications & referencesAccess to 3-oxindoles from Allylic Alcohols and Indoles.Reference Chemistry a European Journal, March 2018Asymmetric Total Synthesis of Lancifodilactone G Acetate.Reference The Journal of Organic Chemistry, March 2018Preparation of Functionalized α,β-Unsaturated Sulfonamides via Olefin Cross-Metathesis.Reference Org. Lett. 2020, 22, 13, 4970–4973Formal Synthesis of (±)-Aplykurodinone-1 Based on the Indium-Catalyzed Conia-Ene Reaction.Reference Synlett 2020; 31(14) 1404-1408Polymer Chain Editing Functionality 'Knock-in', 'Knock-out' and Replacement via Cross Metathesis Reaction and Thiol-Michael Addition.Reference Polym. Chem. 2020,11, 4807-4817Selectively Depolymerizable Polyurethanes from Unsaturated Polyols Cleavable by Olefin Metathesis.Reference Macromol Rapid Commun 2020 ASAP (DOI 10.1002/marc.202000571) PubChem SID:488197712 PubChem SID url:https//pubchem.ncbi.nlm.nih.gov/substance/488197712 IUPAC Name:[1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-dichloro-[(2-propan-2-yloxyphenyl)methylidene]ruthenium INCHI:InChI=1S/C21H26N2.C10H12O.2ClH.Ru/c1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6;1-8(2)11-10-7-5-4-6-9(10)3;;;/h9-12H,7-8H2,1-6H3;3-8H,1-2H3;2*1H;/q;;;;+2/p-2 InChi Key:ZRPFJAPZDXQHSM-UHFFFAOYSA-L Canonical SMILES:CC1=CC(=C(C(=C1)C)N2CCN(C2=[Ru](=CC3=CC=CC=C3OC(C)C)(Cl)Cl)C4=C(C=C(C=C4C)C)C)C Isomeric SMILES:CC1=CC(=C(C(=C1)C)N2CCN(C2=[Ru](=CC3=CC=CC=C3OC(C)C)(Cl)Cl)C4=C(C=C(C=C4C)C)C)C WGK Germany:3 PubChem CID:11763533 敏感性:对光和空气敏感 熔点:216-220°C 象形图: 信号词:Warning 危险声明:H315 Causes skin irritationH319 Causes serious eye irritationH413 May cause long lasting harmful effects to aquatic lifeH302 Harmful if swallowedH312 Harmful in contact with skinH332 Harmful if inhaled 预防措施声明:P261,P305+P351+P338,P273,P280,P302+P352,P321,P501,P264,P271,P270,P304+P340,P362+P364,P330,P264+P265,P301+P317,P317,P337+P317,P332+P317 个人防护装备:Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter 产品包装
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