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Methyl 3-iodobenzoate

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Methyl 3-iodobenzoate manufacturers

  • Methyl 3-iodobenzoate
  • Methyl 3-iodobenzoate pictures
  • $100.00
  • 2024-04-25
  • CAS:618-91-7
  • Min. Order: 1kg
  • Purity: 99.93%
  • Supply Ability: 1000kg per week
Methyl 3-iodobenzoate Basic information
Product Name:Methyl 3-iodobenzoate
Synonyms:RARECHEM AL BF 0709;M-IODOBENZOIC ACID METHYL ESTER;3-iodo-benzoicacimethylester;3-Iodomethylbenzoate;Benzoic acid, m-iodo-, methyl ester;Benzoicacid,3-iodo-,methylester;DPPE1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine;Methyl m-iodobenzoate
CAS:618-91-7
MF:C8H7IO2
MW:262.04
EINECS:210-570-4
Product Categories:Aromatic Esters;API intermediates;Acids & Esters;Iodine Compounds
Mol File:618-91-7.mol
Methyl 3-iodobenzoate Structure
Methyl 3-iodobenzoate Chemical Properties
Melting point 46-50 °C
Boiling point 277°C (rough estimate)
density 1.7835 (estimate)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
form solid
color Yellow-brown
InChI1S/C8H7IO2/c1-11-8(10)6-3-2-4-7(9)5-6/h2-5H,1H3
InChIKeyNPXOIGSBRLCOSD-UHFFFAOYSA-N
SMILESCOC(=O)c1cccc(I)c1
CAS DataBase Reference618-91-7(CAS DataBase Reference)
NIST Chemistry ReferenceBenzoic acid, 3-iodo-, methyl ester(618-91-7)
EPA Substance Registry SystemBenzoic acid, 3-iodo-, methyl ester (618-91-7)
Safety Information
Hazard Codes Xi,N
Risk Statements 41-51/53
Safety Statements 53-26-39-61
RIDADR 3077
WGK Germany 2
TSCA TSCA listed
HazardClass IRRITANT
PackingGroup Ⅲ
HS Code 29163900
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Dam. 1
MSDS Information
Methyl 3-iodobenzoate Usage And Synthesis
Chemical PropertiesPale yellow crystals
Synthesis
Methanol

67-56-1

3-Iodobenzoic acid

618-51-9

Methyl 3-iodobenzoate

618-91-7

The general procedure for the synthesis of methyl 3-iodobenzoate from methanol and 3-iodobenzoic acid was as follows: 3-iodobenzoic acid (50 g, 0.20 mol) was dissolved in 300 mL of methanol, followed by the addition of 1 mL of concentrated sulfuric acid as a catalyst. The reaction mixture was heated to reflux at 80 °C for 24 hours. During the reaction, the water generated from the reaction was removed by distillation and methanol was replenished twice to maintain the reaction volume. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the solvent was removed by distillation under reduced pressure. 600 mL of ether was added to the residue and stirred overnight to induce the product to precipitate as a white precipitate. The product was separated by filtration and washed with cold water to afford methyl 3-iodobenzoate (51.3 g, 97% yield) as a white solid. NMR hydrogen spectrum (300MHz, CDCl3): δ8.34 (s, 1H), 7.97 (d, J=7.5Hz, 1H), 7.85 (d, J=7.2Hz, 1H), 7.15 (td, J1=7.8Hz, J2=2.7Hz, 1H), 3.89 (s, 3H). Gas chromatography-mass spectrometry (GC-MS) analysis: the calculated value of the molecular ion peak (m/z) C8H7IO2 was 262.0 and the measured value was 262.0.

References[1] Journal of Organic Chemistry, 2012, vol. 77, # 7, p. 3197 - 3214
[2] Patent: WO2014/11477, 2014, A1. Location in patent: Page/Page column 29; 30
[3] Patent: WO2010/149620, 2010, A1. Location in patent: Page/Page column 45
[4] Journal of Medicinal Chemistry, 2012, vol. 55, # 22, p. 9562 - 9575
[5] Patent: JP5725475, 2015, B2. Location in patent: Paragraph 0028; 0029
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