Name | 2-Chloro-4-Iodobenzene | CAS# | 153034-86-7 | |
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Price | ¥Inquiry/1kg ¥Inquiry/250g | Purity | 99.0% | |
Stocking Period |
3 Day | Stock | In Stock |
Detail
Product Information
Chemical Name: 2-Chloro-4-iodopyridine CAS: 153034-86-7 Assay: % min Molecular formula:C5H3ClIN Molecular weight:239.44 EINECS: 628-020-0 2-Chloro-4-iodopyridine Properties Melting Point 42-43 °C (lit.) Boiling Point 255.5±20.0 °C(Predicted) Density 2.052±0.06 g/cm3(Predicted) Refractive Index 1.642 Flash point 1110 °C Storage Condition Keep in dark place,Sealed in dry,Room Temperature Solubility Chloroform, Ethyl Acetate Appearance Crystals or Crystalline Flakes Acidity Coefficient (pKa) -0.03±0.10(Predicted) Color White to yellow Odor PH Water Solubility
Merck BRN 108668 Stability Oxide, light InChIKey Security Information Dangerous Goods Sign Xn,Xi Hazard Category Code 22-41-43-36/37/38-20/22 Safety Instructions 26-36/37/39-36-22 Dangerous Goods Transportation No UN2811 WGK Germany 3 RTECS F Hazard Note Irritant/Light Sensitive TSCA Hazard Level Irritant/Light Sensitive Packaging Category HS CODE 29339900 Toxic substance data Toxicity 2-Chloro-4-iodopyridine Application and Synthesis Chemical Property: Usage 1: Usage 2 : Usage 3 : Usage 4 : Production Method: Yield:95% Synthesis conditions:With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 3 h; Experimental procedure:A solution of 2-chloro-3-iodopyridine (12 g, 50 mmol) in 20 mL of THF was slowly added to a cold (−78 °C) lithium diisopropylamide solution (prepared by adding 1.6 M n-butyllithium ( 31.25) A solution of ML, 50mmol) in hexane was added to a solution of diisopropylamine (7mL, 50mmol) in THF (100mL). After 3 hours, water (20mL) was added to the mixture and extracted with diethyl ether (2×100mL). . The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo (20 °C) to give a brown solid, which was purified by filtration over silica (ethyl acetate/heptane 8/2), yield: 95% (11.4 g). ), pale yellow needles. 1H NMR (CDCl3): 8 8.07 (d, J = 5.3Hz, 1H), 7.76 (d, J = 1.1Hz, 1H), 7.59 (dd, J = 5.0/0.11. Hz, 1H ).13C NMR (CDCl3): δ 151.7, 149.6, 133.0, 131.5, 106.6. MS (EI) m/z 240 (M+1). More
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