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2-Iodotoluene

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2-Iodotoluene manufacturers

  • 2-Iodotoluene
  • 2-Iodotoluene pictures
  • $120.00
  • 2026-11-04
  • CAS:615-37-2
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 20 tons
  • 2-Iodotoluene
  • 	2-Iodotoluene pictures
  • $100.00
  • 2026-09-02
  • CAS:615-37-2
  • Min. Order: 1KG
  • Purity: 99%
  • 2-Iodotoluene
  • 2-Iodotoluene pictures
  • $15.00
  • 2021-07-13
  • CAS:615-37-2
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
2-Iodotoluene Basic information
Synthesis
Product Name:2-Iodotoluene
Synonyms:Toluene,o-iodo-;2-IODOTOLUENE;1-Iodo-2-methylbenzene,;O-IODOTOLUENE;2-Iodotoluene98%;2-Iodotoluene (stabilized with Copper chip);(2-Methylphenyl) iodide;2-Methyl-1-iodobenzene
CAS:615-37-2
MF:C7H7I
MW:218.04
EINECS:210-422-9
Product Categories:alkyl Iodine;Aromatic Hydrocarbons (substituted) & Derivatives;Halogen toluene;Iodine Compounds
Mol File:615-37-2.mol
2-Iodotoluene Structure
2-Iodotoluene Chemical Properties
Melting point 11.27°C (estimate)
Boiling point 211 °C
density 1.72
refractive index 1.61
Fp 90 °C - closed cup
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Sparingly), Methanol (Slightly)
form clear liquid
color Colorless to Red to Green
Specific Gravity1.713
Sensitive Light Sensitive
BRN 1634294
InChI1S/C7H7I/c1-6-4-2-3-5-7(6)8/h2-5H,1H3
InChIKeyRINOYHWVBUKAQE-UHFFFAOYSA-N
SMILESCc1ccccc1I
CAS DataBase Reference615-37-2(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 1-iodo-2-methyl-(615-37-2)
EPA Substance Registry SystemBenzene, 1-iodo-2-methyl- (615-37-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37-36/37/39-27
RIDADR UN 2810
WGK Germany 3
TSCA TSCA listed
HazardClass IRRITANT
HS Code 29036990
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
MSDS Information
ProviderLanguage
o-Iodotoluene English
SigmaAldrich English
ACROS English
ALFA English
2-Iodotoluene Usage And Synthesis
Synthesis

Method 1,
Synthesis of 615-37-2_1
0.2 mL of cuprous oxide/NH3 catalytic system, 135.8 mg of o-methylphenylboronic acid, 0.830 g of potassium iodide, and 2 mL of water were added to a round-bottom flask equipped with a magnetic stirrer. The system was left open at room temperature for 24 hours. After the reaction was complete, 1.5 mL of 2 mol/L sodium hydroxide solution was added, and the mixture was extracted three times with 2 mL of dichloromethane each time. The combined organic phases were concentrated to give 176 mg of 2-iodotoluene, with a yield of 81%. Method 2,
Synthesis of 615-37-2_2
Accurately weigh o-bromotoluene (42.8 mg, 0.25 mmol), tetramethylammonium iodide (150.79 mg, 0.75 mmol), cuprous oxide (3.6 mg, 0.025 mmol), and L-proline (5.8 mg, 0.05 mmol), and add them sequentially to a 25 mL Schlenk flask. Add purified ethanol (1.5 mL) and react in a 110 °C oil bath for 30 h. After the reaction is complete, filter the reaction solution through a silica gel column into a 10 mL volumetric flask, and quantify the solution volume to the specified mark with ethyl acetate. Gas chromatography analysis showed that the yield of 2-iodotoluene was 28%.

Chemical PropertiesLiquid
Usessuzuki reaction
Uses2-Iodotoluene is used as a reagent in the synthesis of aryl substituted quinones as β-secretase inhibitors.
DefinitionChEBI: An iodoarene that is 2-methylbenzene substituted by an iodo group at position 1.
Tag:2-Iodotoluene(615-37-2) Related Product Information
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