ChemicalBook--->CAS DataBase List--->289039-82-3

289039-82-3

289039-82-3 Structure

289039-82-3 Structure
IdentificationBack Directory
[Name]

METHYL 5-CHLORO-2-IODOBENZOATE
[CAS]

289039-82-3
[Synonyms]

METHYL 5-CHLORO-2-IODOBENZOATE
5-chloro-2-iodo-Benzoic acid Methyl ester
Benzoic acid, 5-chloro-2-iodo-, methyl ester
[Molecular Formula]

C8H6ClIO2
[MDL Number]

MFCD00144772
[MOL File]

289039-82-3.mol
[Molecular Weight]

296.49
Chemical PropertiesBack Directory
[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
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C8H6ClIO2/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4H,1H3
[InChIKey]

LNCNRPALSKTJBG-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC(Cl)=CC=C1I
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS08,GHS09
[Signal word ]

Warning
[Hazard statements ]

H320-H351-H336-H410
[Precautionary statements ]

P501-P261-P273-P202-P201-P271-P264-P280-P391-P308+P313-P337+P313-P305+P351+P338-P304+P340+P312-P403+P233-P405
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 5-CHLORO-2-IODOBENZOATE(289039-82-3)1HNMR
Hazard InformationBack Directory
[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
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