Cas no 172418-32-5 (trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst)
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
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
-
Warning Statement:
P264Thoroughly clean after treatment
P280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective mask
P305If it enters the eyes
P351Rinse carefully with water for a few minutes
P338Remove the contact lens(If any)And easy to operate,Continue flushing
P337If eye irritation persists
P313Obtain medical advice/care - Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: 36/37/38
- Safety Instruction: S26-S36
-
Hazardous Material Identification:
- Safety Term:S26-36/37/39;S36
- Risk Phrases:R36/37/38
- Storage Condition:Argon filled storage
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 >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-KV681-200mg |
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst |
172418-32-5 | 98%,Pd>22.65% | 200mg |
¥228.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-KV681-1g |
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst |
172418-32-5 | 98%,Pd>22.65% | 1g |
¥681.0 | 2022-06-10 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 671916-1G |
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst |
172418-32-5 | 1g |
¥1657.96 | 2023-11-30 | ||
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 671916-5G |
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst |
172418-32-5 | 5g |
¥6979.25 | 2023-11-30 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | D819998-5g |
trans-Di-mu-acetatobis[2-(di-o-tolylphosphino)benzyl]dipalladium(II) |
172418-32-5 | 98% | 5g |
¥3,744.00 | 2022-01-10 | |
| TRC | B400625-250mg |
trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) [Hermann’s Catalyst] |
172418-32-5 | 250mg |
$ 155.00 | 2023-04-18 | ||
| TRC | B400625-1g |
trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) [Hermann’s Catalyst] |
172418-32-5 | 1g |
$ 225.00 | 2022-06-07 | ||
| TRC | B400625-2.5g |
trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) [Hermann’s Catalyst] |
172418-32-5 | 2.5g |
$ 586.00 | 2023-04-18 | ||
| TRC | B400625-5g |
trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) [Hermann’s Catalyst] |
172418-32-5 | 5g |
$ 740.00 | 2022-06-07 | ||
| abcr | AB128853-250 mg |
trans-Di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II), 97%; . |
172418-32-5 | 97% | 250 mg |
€60.90 | 2023-07-20 |
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst Production Method
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst Suppliers
trans-Bis(acetato)biso-(di-o-tolylphosphino)benzyldipalladium(II) Hermann’s Catalyst Related Literature
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Lauren R. Donaldson,Stephen Wallace,David Haigh,E. Elizabeth Patton,Alison N. Hulme Org. Biomol. Chem. 2011 9 2233
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Yang Ran,Yunlong Guo,Yunqi Liu Mater. Horiz. 2020 7 1955
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Simiao Yu,Fuchuan Liu,Jianwei Yu,Shiming Zhang,Clement Cabanetos,Yongqian Gao,Wei Huang J. Mater. Chem. C 2017 5 29
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Bibi Amna,Humaira Masood Siddiqi,Abbas Hassan,Turan Ozturk RSC Adv. 2020 10 4322
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Paolo Innocenti,Hannah Woodward,Lisa O'Fee,Swen Hoelder Org. Biomol. Chem. 2015 13 893
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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