Home Cart Sign in  
Chemical Structure| 30754-23-5 Chemical Structure| 30754-23-5

Structure of 30754-23-5

Chemical Structure| 30754-23-5

Heptakis(6-iodo-6-deoxy)-β-cyclodextrin

CAS No.: 30754-23-5

4.5 *For Research Use Only !

Cat. No.: A146797 Purity: 98%

Change View

Size Price

US Stock

Global Stock

In Stock
100mg łďǶÊÊ Inquiry Inquiry
250mg łÇËǶÊÊ Inquiry Inquiry
1g ł§ďò¶ÊÊ Inquiry Inquiry

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • 100mg

    łďǶÊÊ

  • 250mg

    łÇËǶÊÊ

  • 1g

    ł§ďò¶ÊÊ

In Stock

- +

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Product Citations

Davis, Bradley A. ; Bennett, Jeffrey A. ; Genzer, Jan ; Efimenko, Kirill ; Abolhasani, Milad ;

Abstract: The intersection of heterogeneous catalysis and flow chem. is of great importance for the emerging distributed manufacturing of specialty chems. Specifically, continuous production of aryl amines is an essential step for on-demand and on-site manufacturing of fine chems. This work presents a heterogeneous flow chem. route for accelerated chemoselective hydrogenation of nitroarenes using a poly(β-cyclodextrin) network-supported palladium catalyst. The developed packed-bed flow reactor enables the selective hydrogenation of a rationally selected library of nitroarenes with >99% yield at room temperature and short residence times (1 min). Utilizing sodium borohydride as the hydrogen carrier in a pressurized packed-bed flow reactor allows safe and efficient delivery of hydrogen to nitroarene mols. We demonstrate the robustness and versatility of the flow reactor packed with the network-supported catalyst through its consistently high reaction yield over a 3 day run and its reusability and stability in several solvent mixtures with a single-reactor aryl amine manufacturing throughput of up to 31.5 g/day. Furthermore, the catalytic packed-bed reactor is used in a case study for a two-step telescopic synthesis of a critical intermediate for the antibacterial drug linezolid, further supporting its utility as an industrially relevant catalyst for the broad application of catalytic hydrogenations in flow.

Keywords: heterogeneous catalysis ; flow chemistry ; network-supported catalysis ; transfer hydrogenation ; process intensification

Purchased from AmBeed:

Alternative Products

Product Details of [ 30754-23-5 ]

CAS No. :30754-23-5
Formula : C42H63I7O28
M.W : 1904.26
SMILES Code : IC[C@@H]1[C@]2([H])[C@@H]([C@@H](O)[C@](O[C@]3([H])[C@H](O[C@@](O[C@]4([H])[C@H](O[C@@](O[C@]5([H])[C@H](O[C@@](O[C@@]6([H])[C@H](O)[C@@H](O)[C@@](O[C@@H]6CI)([H])O[C@@]7([H])[C@H](O)[C@@H](O)[C@@](O[C@@H]7CI)([H])O[C@@]8([H])[C@H](O)[C@@H](O)[C@@](O[C@@H]8CI)([H])O2)([H])[C@H](O)[C@H]5O)CI)([H])[C@H](O)[C@H]4O)CI)([H])[C@H](O)[C@H]3O)CI)([H])O1)O
MDL No. :MFCD00803290
InChI Key :YODKQJPYQJRHEQ-FOUAGVGXSA-N
Pubchem ID :11105283

Safety of [ 30754-23-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 30754-23-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 30754-23-5 ]

[ 30754-23-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 30754-23-5 ]
  • [ 160661-60-9 ]
References: [1] Chemical Communications, 2012, vol. 48, # 65, p. 8063 - 8065.
[2] Chemical Communications, 2014, vol. 50, # 79, p. 11757 - 11759.
 

Historical Records

Categories