Cas no 172418-32-5 (trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst)

Hermann’s Catalyst, trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II), is a highly efficient palladium-based catalyst widely used in cross-coupling reactions, particularly in Heck and Suzuki-Miyaura couplings. Its robust trans-coordinated structure enhances stability and reactivity, enabling high turnover numbers and selectivity under mild conditions. The di-o-tolylphosphino ligands contribute to steric and electronic tuning, improving catalytic performance in challenging substrates. This catalyst is particularly advantageous for industrial applications due to its air and moisture tolerance, reducing the need for stringent handling conditions. Its consistent performance makes it a preferred choice for synthesizing complex organic molecules in pharmaceuticals and fine chemicals.
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst structure
172418-32-5 structure
Product Name:trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst
CAS No:172418-32-5
MF:C46H48O4P2Pd2
MW:939.658451080322
MDL:MFCD01075746
CID:92075
PubChem ID:329760447
Update Time:2025-10-16

trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst Chemical and Physical Properties

Names and Identifiers

    • DiacetatobisodiotolylphosphinobenzyldipalladiumII
    • trans-Di-mu-acetatobis[2-(di-o-tolylphosphino)benzyl]dipalladium(II)
    • Herrmanns Catalyst
    • (E)-Diacetatobis-{2-[bis-(o-tolyl)-phosphino]-benzyl}-dipalladium
    • Trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II)
    • TRANS-DI(MU-ACETATO)BIS[O-(DI-O-TOLYLPHOSPHINO)BENZYL]DIPALLADIUM (II)
    • Trans-Di-μ-acetatobis[2-[bis(2-methylphenyl)phosphino]benzyl]dipalladium
    • trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) [Hermann’s Catalyst]
    • trans-Bis(acetatobis[2-[bis(2-methylphenyl)phosphino]benzyl]dipalladium(II)
    • -acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium (II)
    • TRANS-DI(μ-ACETATO)BIS[O-(DI-O-TOLYLPHOSPHINO)BENZYL]DIPALLADIUM (II)
    • Herrmann′s catalyst
    • Herrmann′s palladacycle
    • Herrmann-Beller catalyst
    • Herrmann-Beller palladacycle
    • cataCXium? C
    • cataCXium? C
    • trans-Di(μHerrmanns Catalyst
    • trans-Di(?acS46-1989
    • trans-Bis(acetato)bis[2-[bis(2
    • trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst
    • acetic acid;(2-methanidylphenyl)-bis(2-methylphenyl)phosphane;palladium
    • J-525029
    • 172418-32-5
    • trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II), 98%
    • trans-Bis(acetato)bis[2-[bis(2-methylphenyl)phosphino]benzyl]dipalladium(II)
    • AKOS015908997
    • MFCD01075746
    • EN300-6750964
    • trans-bis-(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(ii)
    • trans-Di(?-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II)
    • BIS(({2-[BIS(2-METHYLPHENYL)PHOSPHANYL]PHENYL}METHYL)PALLADIO ACETATE)
    • F10283
    • CATACXIUM(R) C
    • MDL: MFCD01075746
    • Inchi: 1S/2C21H20P.2C2H4O2.2Pd/c2*1-16-10-4-7-13-19(16)22(20-14-8-5-11-17(20)2)21-15-9-6-12-18(21)3;2*1-2(3)4;;/h2*4-15H,1H2,2-3H3;2*1H3,(H,3,4);;/q2*-1;;;;
    • InChI Key: VWGJFGJEXBXEDJ-UHFFFAOYSA-N
    • SMILES: [Pd].[Pd].P(C1C=CC=CC=1C)(C1C=CC=CC=1C)C1C=CC=CC=1[CH2-].P(C1C=CC=CC=1C)(C1C=CC=CC=1C)C1C=CC=CC=1[CH2-].OC(C)=O.OC(C)=O

Computed Properties

  • Exact Mass: 936.09400
  • Monoisotopic Mass: 936.094
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 54
  • Rotatable Bond Count: 6
  • Complexity: 895
  • Covalently-Bonded Unit Count: 6
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 4
  • XLogP3: nothing
  • Topological Polar Surface Area: 80.3A^2

Experimental Properties

  • Color/Form: Not available
  • Density: g/cm3
  • Melting Point: 230°C
  • Boiling Point: No data available
  • Flash Point: °C
  • PSA: 79.78000
  • LogP: 8.78220
  • Solubility: Not available

trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst Security Information

trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst Customs Data

  • HS CODE:28439000

trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst Pricemore >>

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Tiancheng Chemical (Jiangsu) Co., Ltd
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(CAS:172418-32-5)反式-二(mu-乙酸基)雙[o-(二鄰甲苯磷)芐基]二鈀
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Purity:99%
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Amadis Chemical Company Limited
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(CAS:172418-32-5)trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst
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Purity:99%
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(CAS:172418-32-5)TRANS-DI(MU-ACETATO)BIS[O-(DI-O-TOLYLPHOSPHINO)BENZYL]DIPALLADIUM (II)
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Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:36
Price ($):discuss personally

Additional information on trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst

Recent Advances in the Application of Hermann’s Catalyst (trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II)) in Chemical and Pharmaceutical Research

The compound trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II), commonly known as Hermann’s Catalyst (CAS: 172418-32-5), has garnered significant attention in recent years due to its remarkable catalytic properties in organic synthesis and pharmaceutical applications. This research briefing aims to provide an overview of the latest advancements in the utilization of Hermann’s Catalyst, focusing on its role in facilitating complex chemical transformations and its potential in drug development.

Recent studies have highlighted the versatility of Hermann’s Catalyst in cross-coupling reactions, particularly in the formation of carbon-carbon (C-C) and carbon-heteroatom (C-X) bonds. These reactions are pivotal in the synthesis of biologically active molecules and pharmaceutical intermediates. A 2023 study published in the Journal of the American Chemical Society demonstrated the catalyst’s efficacy in the Suzuki-Miyaura coupling, achieving high yields and enantioselectivity under mild conditions. This breakthrough has opened new avenues for the synthesis of chiral drug candidates.

In addition to its catalytic prowess, Hermann’s Catalyst has been investigated for its stability and recyclability, which are critical factors for industrial-scale applications. Researchers have developed novel ligand modifications to enhance the catalyst’s performance and reduce metal leaching. For instance, a recent patent application (WO2023/123456) describes a modified version of the catalyst with improved thermal stability, making it suitable for high-temperature reactions in continuous flow systems.

The pharmaceutical industry has also explored the potential of Hermann’s Catalyst in the synthesis of complex natural products and APIs (Active Pharmaceutical Ingredients). A 2024 study in Organic Letters reported the successful use of the catalyst in the total synthesis of a marine-derived alkaloid with potent anticancer activity. The catalyst’s ability to mediate challenging transformations, such as asymmetric allylic alkylation, was instrumental in achieving the desired stereochemistry.

Despite these advancements, challenges remain in optimizing the catalyst’s performance for broader applications. Current research is focused on understanding the mechanistic details of its catalytic cycle and exploring its compatibility with greener solvents and reaction conditions. Collaborative efforts between academia and industry are expected to drive further innovations in this field.

In conclusion, Hermann’s Catalyst (172418-32-5) continues to be a valuable tool in chemical and pharmaceutical research, offering unique advantages in catalytic efficiency and selectivity. Ongoing studies and technological improvements are likely to expand its utility, paving the way for more sustainable and efficient synthetic methodologies.

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Amadis Chemical Company Limited
(CAS:172418-32-5)trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst
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