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Ethyl 2-iodobenzoate

Ethyl 2-iodobenzoate Suppliers list
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Beijing Ouhe Technology Co., Ltd  
Tel: 13552068683 13522913783
Email: 2355560935@qq.com
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com
Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Tel: 13761987713
Email: hxzheng@sunwaypharm.cn

Ethyl 2-iodobenzoate manufacturers

Ethyl 2-iodobenzoate Basic information
Product Name:Ethyl 2-iodobenzoate
Synonyms:RARECHEM AL BI 0562;ETHYL O-IODOBENZOATE;2-(Ethoxycarbonyl)iodobenzene;E**Ethyl 2-iodobenzoate;Ethyl 2-iodobenzoate
CAS:1829-28-3
MF:C9H9IO2
MW:276.07
EINECS:
Product Categories:Aromatic Esters;Indazoles
Mol File:1829-28-3.mol
Ethyl 2-iodobenzoate Structure
Ethyl 2-iodobenzoate Chemical Properties
Boiling point 163-165°C/23mm
density 1.664±0.06 g/cm3(Predicted)
refractive index 1.584
Fp 163-165°C/23mm
storage temp. 2-8°C(protect from light)
solubility Difficult to mix.
form clear liquid
color Colorless to Light yellow to Light orange
Sensitive Light Sensitive
BRN 2084297
Safety Information
Hazard Codes Xi
HazardClass IRRITANT, LIGHT SENSITIVE
HS Code 2916399090
MSDS Information
ProviderLanguage
ALFA English
Ethyl 2-iodobenzoate Usage And Synthesis
UsesEthyl 2-iodobenzoate is used as anti-infective, contraceptive agent and x-ray contrast medium for diagnostic radiology.
Synthesis
Ethanol

64-17-5

2-Iodobenzoic acid

88-67-5

ETHYL 2-IODOBENZOATE

1829-28-3

General procedure for the synthesis of ethyl 2-iodobenzoate from ethanol and 2-iodobenzoic acid: 2-iodobenzoic acid (10 g) was dissolved in 60 mL of ethanol and 5 mL of concentrated H2SO4 was added as a catalyst. The reaction mixture was placed in an oil bath at 78 °C with electromagnetic stirring for 5 hours. Upon completion of the reaction, excess ethanol was removed under reduced pressure using a rotary evaporator. Water and ethyl acetate were added to the residue to separate the organic layer. The organic layer was washed three times sequentially with water and saturated sodium bicarbonate solution. Finally, the organic layer was dried with anhydrous Na2SO4, filtered and the solvent was removed by distillation to afford ethyl 2-iodobenzoate in 99% yield.

References[1] Synthetic Communications, 2017, vol. 47, # 12, p. 1175 - 1184
[2] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 18, p. 4822 - 4825
[3] Tetrahedron Letters, 2014, vol. 55, # 3, p. 690 - 693
[4] Patent: US2010/216853, 2010, A1. Location in patent: Page/Page column 19-20
[5] Tetrahedron Letters, 1996, vol. 37, # 35, p. 6375 - 6378
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