1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole
- Product Name
- 1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole
- CAS No.
- 575452-22-1
- Chemical Name
- 1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole
- Synonyms
- 1-(1-Ethoxyethyl)-4-iodopyrazole;1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole;1H-Pyrazole, 1-(1-ethoxyethyl)-4-iodo-
- CBNumber
- CB52665431
- Molecular Formula
- C7H11IN2O
- Formula Weight
- 266.08
- MOL File
- 575452-22-1.mol
1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole Property
- Boiling point:
- 74-76 °C(Press: 0.5 Torr)
- Density
- 1.72±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C(protect from light)
- pka
- -0.19±0.10(Predicted)
- Appearance
- Light yellow to yellow Liquid
Safety
- HS Code
- 2933199090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- E676548
- Product name
- 1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- E676548
- Product name
- 1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole
- Packaging
- 50mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- Z0702
- Product name
- 1-(1-Ethoxy-ethyl)-4-iodo-1H-pyrazole
- Packaging
- 1g
- Price
- $103
- Updated
- 2021/12/16
- Product number
- OR307170
- Product name
- 1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole
- Packaging
- 5g
- Price
- $109
- Updated
- 2021/12/16
- Product number
- AK162019
- Product name
- 1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole
- Purity
- 97%
- Packaging
- 1g
- Price
- $38
- Updated
- 2021/12/16
1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole Chemical Properties,Usage,Production
Synthesis
3469-69-0
109-92-2
575452-22-1
Step 1: Suspend 4-iodo-1H-pyrazole (3.0 g) in benzene (150 mL), stir and heat the suspension. Ethyl vinyl ether (4.4 mL) was slowly added, followed by dropwise addition of concentrated hydrochloric acid, with continuous stirring at 60 °C for 3 hours. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure and the residue was neutralized with saturated aqueous sodium bicarbonate (10 mL). The mixture was extracted with ethyl acetate (50 mL) and the extract was washed sequentially with distilled water (100 mL). The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to afford the target compound 1-(1-ethoxyethyl)-4-iodo-1H-pyrazole as a clear yellow liquid (3.0 g, 73% yield). 1H NMR (CDCl3): δ 7.54 (s, 1H), 7.41 (s, 1H), 5.40 (q, 1H, J = 6.0Hz), 3.38-3.18 (m, 2H), 1.54 (d, 3H, J = 6.0Hz), 1.05 (t, 3H, J = 7.1Hz).
References
[1] Organic Letters, 2009, vol. 11, # 9, p. 1999 - 2002
[2] Patent: US2010/190981, 2010, A1. Location in patent: Page/Page column 104
[3] Synthetic Communications, 2011, vol. 41, # 16, p. 2430 - 2434
[4] Heterocycles, 2003, vol. 60, # 4, p. 879 - 886
[5] Organic Letters, 2004, vol. 6, # 26, p. 4929 - 4932
1-(1-Ethoxyethyl)-4-iodo-1H-pyrazole Preparation Products And Raw materials
Raw materials
Preparation Products
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