Basic information Safety Supplier Related

5-Iodo-2-methylbenzoic acid

Basic information Safety Supplier Related

5-Iodo-2-methylbenzoic acid Basic information

Product Name:
5-Iodo-2-methylbenzoic acid
Synonyms:
  • 5-IODO-2-METHYL BENZOIC ACID
  • 5-IODO-2-METHYL BENZOIC ACID 95.0%
  • 5-lodo-2-methyl-Benzoic-acid
  • 5-iodo-methyl-benzoic Acid
  • 5-lodo-2-methylbenzoic acid 98%
  • 5-Iodo-2-Methybenzoic Acid
  • 5-Iodo-2-methylbenzo
  • 5- iodine-2- Methylbenzoic acid
CAS:
54811-38-0
MF:
C8H7IO2
MW:
262.04
EINECS:
611-200-8
Product Categories:
  • Acids & Esters
  • Iodine Compounds
  • BenzoicAcidDerivative
  • bc0001
  • 54811-38-0
Mol File:
54811-38-0.mol
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5-Iodo-2-methylbenzoic acid Chemical Properties

Melting point:
179.0 to 183.0 °C
Boiling point:
339.6±30.0 °C(Predicted)
Density 
1.867±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
3.52±0.25(Predicted)
color 
White to Almost white
InChI
InChI=1S/C8H7IO2/c1-5-2-3-6(9)4-7(5)8(10)11/h2-4H,1H3,(H,10,11)
InChIKey
WUBHOZQZSHGUFI-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC(I)=CC=C1C
CAS DataBase Reference
54811-38-0(CAS DataBase Reference)
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Safety Information

HS Code 
2916399090
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5-Iodo-2-methylbenzoic acid Usage And Synthesis

Chemical Properties

White crystalline powder

Uses

5-Iodo-2-methylbenzoic acid

Synthesis

118-90-1

54811-38-0

O-methylbenzoic acid was used as starting material and reacted with iodic acid and 0.5 equivalents of iodine in the presence of molecular sieves loaded with iron oxide to form the intermediate 5-iodo-2-methylbenzoic acid. After completion of the reaction, the reaction mixture was cooled to room temperature and separated by filtration. The temperature of the mother liquor was lowered to 20 degrees Celsius to induce precipitation of a large amount of solid. At this temperature, the precipitate was mixed with the catalyst and the process could be repeated five times to increase the yield. The filtrate was dissolved to obtain the crude product. The crude product was recrystallized with 2.5 times the volume of solvent, and the process was repeated 5 times, and finally a white crystalline product was obtained by weight of ethyl acrylate, and the yield could be more than 88%.

References

[1] Patent: CN107652175, 2018, A. Location in patent: Paragraph 0054-0098
[2] Patent: EP1642881, 2006, A1. Location in patent: Page/Page column 10
[3] European Journal of Organic Chemistry, 2017, vol. 2017, # 22, p. 3234 - 3239
[4] Patent: CN103980263, 2016, B. Location in patent: Paragraph 0032; 0033
[5] Patent: EP1595862, 2005, A1. Location in patent: Page/Page column 10

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