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| | BIS(TERT-BUTYLCARBONYLOXY)IODOBENZENE 97 Basic information |
| Product Name: | BIS(TERT-BUTYLCARBONYLOXY)IODOBENZENE 97 | | Synonyms: | BIS(TERT-BUTYLCARBONYLOXY)IODOBENZENE 97;(di-tert-butylcarbonyloxyiodo)benzol;(Di-tert-butylcarbonyloxyiodo)benzol, 2,2-Dimethylpropanoic acid, phenyliodine complex, Bis(2,2-dimethylpropanoato-O)phenyliodide, Di-(Pivaloyloxy)iodobenzene;Bis(tert-butylcarbonyloxy)iodobenzene 97%;Iodine, bis(2,2-dimethylpropanoato-κO)phenyl-;phenyl-l3-iodanediyl bis(2,2-dimethylpropanoate);2-(2,2-dimethylpropanoyloxy)-3-iodophenyl]2,2-dimethylpropanoate;[BIS(T-BUTYLCARBONYLOXY)IODO] BENZENE | | CAS: | 57357-20-7 | | MF: | C16H23IO4 | | MW: | 406.26 | | EINECS: | | | Product Categories: | | | Mol File: | 57357-20-7.mol |  |
| | BIS(TERT-BUTYLCARBONYLOXY)IODOBENZENE 97 Chemical Properties |
| Melting point | 104-109 °C | | form | powder to crystal | | color | White to Light yellow |
| WGK Germany | 3 | | HS Code | 2931.90.6000 |
| | BIS(TERT-BUTYLCARBONYLOXY)IODOBENZENE 97 Usage And Synthesis |
| Uses | Rh2(esp)2: An Exceptionally Efficient and Selective Catalyst for C-H Amination
Reagent for:
- Preparation of α,β-unsaturated-γ-lactams via Rh-catalyzed C-H amination of allene carbamates, then Ru-catalyzed cyclocarbonylation
- Palladium-catalyzed diamination
- Preparation of functionalized bicyclic heterocyclic compounds by rhodium-catalyzed allene amidation and cyclization
- Preparation of piperidine and pyrrolidine derivatives via copper-catalyzed intramolecular aminoacetoxylation of aminoolefins
- C-H acyloxylation of arenes
- Hypervalent iodine oxidant
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| | BIS(TERT-BUTYLCARBONYLOXY)IODOBENZENE 97 Preparation Products And Raw materials |
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