2-IODO-1H-INDOLE
- Product Name
- 2-IODO-1H-INDOLE
- CAS No.
- 26340-49-8
- Chemical Name
- 2-IODO-1H-INDOLE
- Synonyms
- 2-IODO-1H-INDOLE;1H-Indole,2-iodo-
- CBNumber
- CB62454849
- Molecular Formula
- C8H6IN
- Formula Weight
- 243.04
- MOL File
- 26340-49-8.mol
2-IODO-1H-INDOLE Property
- Melting point:
- 79-81 °C
- Boiling point:
- 341.7±15.0 °C(Predicted)
- Density
- 1.960±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- solubility
- Chloroform (Slightly), DMSO (Slightly)
- form
- solid
- pka
- 15.57±0.30(Predicted)
- color
- Brown
Safety
- HS Code
- 2933998090
N-Bromosuccinimide Price
- Product number
- I707390
- Product name
- 2-Iodoindole
- Packaging
- 250mg
- Price
- $150
- Updated
- 2021/12/16
- Product number
- I707390
- Product name
- 2-Iodoindole
- Packaging
- 2.5g
- Price
- $1190
- Updated
- 2021/12/16
- Product number
- 2333AB
- Product name
- 2-Iodo-1H-indole
- Packaging
- 5g
- Price
- $1738
- Updated
- 2021/12/16
- Product number
- 70924
- Product name
- 2-Iodoindole
- Packaging
- 10g
- Price
- $2200
- Updated
- 2021/12/16
- Product number
- 2333AB
- Product name
- 2-Iodo-1H-indole
- Packaging
- 250mg
- Price
- $320
- Updated
- 2021/12/16
2-IODO-1H-INDOLE Chemical Properties,Usage,Production
Uses
2-Iodoindole is used in the synthesis of arylthioindole molecules as a class of tubulin polymerization inhibitors. Also used in the synthesis of combretastatin A-4 derivatives.
Synthesis
120-72-9
26340-49-8
General procedure for the synthesis of 2-iodoindole from indole: n-butyllithium (nBuLi, 17 mL, 2.62 M hexane solution, 44.54 mmol) was slowly added to a tetrahydrofuran (THF, 80 mL) solution of indole (5.00 g, 42.68 mmol) at -78 °C. The resulting white suspension was stirred at -78 °C for 0.5 h and then bubbled through carbon dioxide (CO2, gas) for 10 min. The solvent was evaporated at 0 °C (~20 lHPa), the crystalline residue was dissolved in THF (100 mL) and cooled to -78 °C, and tert-butyllithium (tBuLi, 31 mL, 1.46 M pentane solution, 45.26 mmol) was added dropwise. After stirring at -78 °C for 1 h, a THF (80 mL) solution of 1,2-diiodoethane (14.40 g, 51.09 mmol) was added dropwise. Stirring was continued at -78 °C for 1 h. Water (H2O, 5 mL) was then added dropwise and the reaction mixture was slowly warmed to room temperature. The reaction was quenched with saturated aqueous ammonium chloride (NH4Cl, 50 mL). The organic and aqueous layers were separated and the aqueous layer was extracted with ethyl acetate (AcOEt, 2 x 80 mL). The organic layers were combined and washed sequentially with 20% sodium thiosulfate (Na2S2O3, 80 mL) aqueous solution, brine (80 mL), dried with anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure. The residue was purified by recrystallization from hexane/dichloromethane (70:1, 40 mL) to afford 2-iodoindole (7.62 g, 74% yield) as white crystals. The filtrate was concentrated under reduced pressure and the residue was purified by recrystallization from hexane/dichloromethane (70:1, 10 mL) to afford 2-iodoindole (0.56 g, 5% yield) as white crystals. The filtrate was again concentrated under reduced pressure and the residue was purified by recrystallization from hexane/dichloromethane (70:1, 8 mL) to afford 2-iodoindole (0.27 g, 3% yield) as light purple crystals. Finally, the filtrate was concentrated under reduced pressure and the residue was purified by fast chromatography (silica gel, hexane/ethyl acetate = 35:1) to afford 2-iodoindole (0.42 g, 4% yield) as white crystals.The total yield of 2-iodoindole was 86%.
References
[1] Tetrahedron Letters, 1997, vol. 38, # 44, p. 7661 - 7664
[2] Tetrahedron, 2001, vol. 57, # 24, p. 5199 - 5212
[3] Tetrahedron Letters, 2001, vol. 42, # 16, p. 2949 - 2951
[4] Tetrahedron Letters, 2007, vol. 48, # 10, p. 1805 - 1808
[5] Tetrahedron, 2013, vol. 69, # 45, p. 9481 - 9493
2-IODO-1H-INDOLE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2-IODO-1H-INDOLE manufacturers
- Product
- 2-IODO-1H-INDOLE 26340-49-8
- Price
- US $1.00/KG
- Min. Order
- 1g
- Purity
- 98%min
- Supply Ability
- ask
- Release date
- 2019-12-20