ChemicalBook > CAS DataBase List > 2-(4-Iodo-1H-pyrazol-1-yl)ethanol

2-(4-Iodo-1H-pyrazol-1-yl)ethanol

Product Name
2-(4-Iodo-1H-pyrazol-1-yl)ethanol
CAS No.
1408334-75-7
Chemical Name
2-(4-Iodo-1H-pyrazol-1-yl)ethanol
Synonyms
4-Iodo-1H-pyrazole-1-ethanol;2-(4-iodopyrazol-1-yl)ethanol;1H-Pyrazole-1-ethanol, 4-iodo-;2-(4-Iodo-1H-pyrazol-1-yl)ethanol
CBNumber
CB03042122
Molecular Formula
C5H7IN2O
Formula Weight
238.03
MOL File
1408334-75-7.mol
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2-(4-Iodo-1H-pyrazol-1-yl)ethanol Property

storage temp. 
2-8°C(protect from light)
Appearance
White to off-white Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P310Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

AK Scientific
Product number
7856DN
Product name
2-(4-Iodo-1H-pyrazol-1-yl)ethanol
Packaging
1g
Price
$390
Updated
2021/12/16
Ambeed
Product number
A101996
Product name
2-(4-Iodo-1H-pyrazol-1-yl)ethanol
Purity
98%
Packaging
100mg
Price
$21
Updated
2021/12/16
Ambeed
Product number
A101996
Product name
2-(4-Iodo-1H-pyrazol-1-yl)ethanol
Purity
98%
Packaging
250mg
Price
$41
Updated
2021/12/16
Ambeed
Product number
A101996
Product name
2-(4-Iodo-1H-pyrazol-1-yl)ethanol
Purity
98%
Packaging
1g
Price
$111
Updated
2021/12/16
Chemenu
Product number
CM127342
Product name
2-(4-iodo-1H-pyrazol-1-yl)ethan-1-ol
Purity
95+%
Packaging
1g
Price
$122
Updated
2021/12/16
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2-(4-Iodo-1H-pyrazol-1-yl)ethanol Chemical Properties,Usage,Production

Synthesis

3469-69-0

540-51-2

1408334-75-7

General procedure: preparation of 2-(4-iodo-1H-pyrazol-1-yl)ethanol 4-Iodo-1H-pyrazole (4.50 g, 23.20 mmol) was dissolved in N,N-dimethylformamide (DMF, 45 mL), and sodium hydride (60% w/w, 1.42 g, 35.5 mmol) was added at 0 °C and stirred at room temperature for 1 hour. Subsequently, 2-bromoethanol (2.5 mL, 35.2 mmol) was added dropwise to the reaction mixture at 0 °C. The reaction system was warmed up to 65 °C and stirred continuously for 3 days. Upon completion of the reaction, the reaction was quenched with saturated sodium chloride solution and ethyl acetate (EtOAc) and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed sequentially with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography using cyclohexane/ethyl acetate (0 to 50% gradient) as eluent to afford the target compound 2-(4-iodo-1H-pyrazol-1-yl)ethanol (3.55 g, 64% yield). 1H NMR (500 MHz, CDCl3): δ 7.55 (s, 1H), 7.52 (s, 1H), 4.32-4.22 (m, 2H), 4.04-3.95 (m, 2H), 2.79-2.68 (br m, 1H). LCMS (ESI) Rt = 1.50 min, MS m/z 238 [M + H]+.

References

[1] Patent: WO2014/37750, 2014, A1. Location in patent: Paragraph 00142-00144

2-(4-Iodo-1H-pyrazol-1-yl)ethanol Preparation Products And Raw materials

Raw materials

Preparation Products

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1408334-75-7, 2-(4-Iodo-1H-pyrazol-1-yl)ethanolRelated Search:


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