METHYL 5-CHLORO-2-IODOBENZOATE

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Products Intro: Product Name:METHYL 5-CHLORO-2-IODOBENZOATE
CAS:289039-82-3
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CAS:289039-82-3
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Products Intro: Product Name:Benzoic acid, 5-chloro-2-iodo-, Methyl ester
CAS:289039-82-3
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Products Intro: Product Name:methyl 5-chloro-2-iodobenzoate
CAS:289039-82-3
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Products Intro: Product Name:METHYL 5-CHLORO-2-IODOBENZOATE
CAS:289039-82-3
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METHYL 5-CHLORO-2-IODOBENZOATE manufacturers

METHYL 5-CHLORO-2-IODOBENZOATE Basic information
Product Name:METHYL 5-CHLORO-2-IODOBENZOATE
Synonyms:METHYL 5-CHLORO-2-IODOBENZOATE;Benzoic acid, 5-chloro-2-iodo-, methyl ester;5-chloro-2-iodo-Benzoic acid Methyl ester;Benzoic acid, 5-chloro-2-iodo-, methyl ester (9CI, ACI);5-chloro-2-iodo-Benzoic acid methyl ester (9CI ACI)
CAS:289039-82-3
MF:C8H6ClIO2
MW:296.49
EINECS:
Product Categories:Acids & Esters;Chlorine Compounds;Iodine Compounds
Mol File:289039-82-3.mol
METHYL 5-CHLORO-2-IODOBENZOATE Structure
METHYL 5-CHLORO-2-IODOBENZOATE Chemical Properties
Boiling point 295.6±20.0 °C(Predicted)
density 1.837±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C8H6ClIO2/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4H,1H3
InChIKeyLNCNRPALSKTJBG-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC(Cl)=CC=C1I
Safety Information
MSDS Information
METHYL 5-CHLORO-2-IODOBENZOATE Usage And Synthesis
Synthesis
Methanol

67-56-1

5-Chloro-2-iodobenzoic acid

13421-00-6

METHYL 5-CHLORO-2-IODOBENZOATE

289039-82-3

General procedure for the synthesis of methyl 5-chloro-2-iodobenzoate from methanol and 5-chloro-2-iodobenzoic acid: a mixture of 5-chloro-2-iodobenzoic acid (3.0 g, 10.62 mmol), dichlorosulfoxide (12 mL), and N,N-dimethylformamide (0.6 mL) was gently heated with a heat gun until a homogeneous solution was formed (about 15 minutes). Subsequently, the reaction solution was continued to be stirred at 23 °C for 30 min, after which the solvent was removed by concentration under reduced pressure. Methanol (24 mL) was added to the crude product and stirred at 23 °C for 30 min. After the reaction was completed, the reaction solution was again concentrated under reduced pressure. The crude product was purified by rapid chromatography on a Biotage silica gel column with a gradient of cyclohexane to cyclohexane:ethyl acetate (85:15) as eluent to give methyl 5-chloro-2-iodobenzoate (3.02 g, 10.20 mmol, 96% yield).UPLC-MS analysis showed a retention time of 1.17 min and a molecular ion peak m/z 296.6 [M + H]+ , analyzed by method 12.

References[1] Patent: WO2015/91685, 2015, A1. Location in patent: Page/Page column 69
[2] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 10, p. 2823 - 2827
[3] Angewandte Chemie - International Edition, 2013, vol. 52, # 28, p. 7177 - 7180
METHYL 5-CHLORO-2-IODOBENZOATE Preparation Products And Raw materials
Raw materials5-Chloro-2-iodobenzoic acid-->Benzoyl chloride, 5-chloro-2-iodo--->Methanol-->Thionyl chloride-->N,N-Dimethylformamide-->Iodomethane
Tag:METHYL 5-CHLORO-2-IODOBENZOATE(289039-82-3) Related Product Information
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