- 5,6-Dimethoxyindole
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- $0.00 / 1kg
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2023-12-04
- CAS:14430-23-0
- Min. Order: 1kg
- Purity: 99% hplc
- Supply Ability: 1000 kg
- 5,6-Dimethoxyindole
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- $0.00 / 1kg
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2022-10-18
- CAS:14430-23-0
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1Ton
- 5,6-DIMETHOXYINDOLE
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- $100.00 / 1kg
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2022-10-01
- CAS:14430-23-0
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 100 tons
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| 5,6-Dimethoxyindole Basic information |
Product Name: | 5,6-Dimethoxyindole | Synonyms: | 5,6-Dimethoxyindole,99%;5,6-Dimethoxy-1H-indole 99%;5,6-Dimethoxy-1H-indole99%;AKOS JY2083477;5,6-DIMETHOXYINDOLE;1H-Indole, 5,6-dimethoxy-;5,6-Dimethoxyindole 99%;5,6-DIMETHOXY-1H-INDOLE | CAS: | 14430-23-0 | MF: | C10H11NO2 | MW: | 177.2 | EINECS: | 238-402-5 | Product Categories: | Amines;Aromatics;Heterocyclic Compounds;Indole Derivatives;Building Blocks;Heterocyclic Building Blocks;Indoles;Indoles and derivatives;Indoline & Oxindole | Mol File: | 14430-23-0.mol | |
| 5,6-Dimethoxyindole Chemical Properties |
Melting point | 154-157 °C (lit.) | Boiling point | 198°C 8mm | density | 1.182±0.06 g/cm3(Predicted) | Fp | 198°C/8mm | storage temp. | Sealed in dry,Room Temperature | pka | 16.93±0.30(Predicted) | form | Powder | color | Beige | Water Solubility | Insoluble in water. | λmax | 306nm(EtOH)(lit.) | BRN | 5683 | InChIKey | QODBZRNBPUPLEZ-UHFFFAOYSA-N | CAS DataBase Reference | 14430-23-0(CAS DataBase Reference) |
Hazard Codes | Xi | Safety Statements | 22-24/25 | WGK Germany | 3 | F | 10 | HazardClass | IRRITANT | HS Code | 29339900 |
| 5,6-Dimethoxyindole Usage And Synthesis |
Chemical Properties | Beige powder | Uses | 5,6-Dimethoxyindole is an indole derivative as analgesic antiinflammatory. It was used in the synthesis of N-benzyl-N-cyclopropyl-5,6-dimethoxyindole-3-glyoxalamide. | Application | 5,6-Dimethoxyindole was used in the synthesis of N-benzyl-N-cyclopropyl-5,6-dimethoxyindole-3-glyoxalamide. Reactant in synthesis of indolylhydroxyoxindoles via enantioselective Friedel-Crafts reaction Reactant in synthesis of benzyl trimethoxyindoles Reactant for synthesis of benzoylpiperazinyl-indolyl ethane dione derivatives as HIV-1 inhibitors Reactant for synthesis of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors Reactant for preparation of tryptophanol derivatives via the Grignard reaction | Synthesis Reference(s) | Journal of the American Chemical Society, 75, p. 5887, 1953 DOI: 10.1021/ja01119a030 Synthesis of 5,6-Dimethoxyindoles and 5,6-Dimethoxyoxindoles. A New Synthesis of Indoles DOI: 10.1021/ja01619a049 |
| 5,6-Dimethoxyindole Preparation Products And Raw materials |
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