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2-IODO-5-METHYLBENZOIC ACID

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CAS:52548-14-8
Purity:98% Package:100g;|1000g
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CAS:52548-14-8
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CAS:52548-14-8
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Products Intro: Product Name:2-Iodo-5-methylbenzoic acid
CAS:52548-14-8
Purity:98%(Min,HPLC) Package:1G;1KG;100KG

2-IODO-5-METHYLBENZOIC ACID manufacturers

  • 2-IODO-5-METHYLBENZOIC ACID
  • 2-IODO-5-METHYLBENZOIC ACID pictures
  • $100.00 / 1KG
  • 2025-09-25
  • CAS:52548-14-8
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
2-IODO-5-METHYLBENZOIC ACID Basic information
Product Name:2-IODO-5-METHYLBENZOIC ACID
Synonyms:2-IODO-5-METHYLBENZOIC ACID,97+%;3-Carboxy-4-iodotoluene, 6-Iodo-m-toluic acid;Benzoic acid,2-iodo-5-Methyl-;3-Carboxy-4-iodotoluene;5-Methyl-2-iodobenzoic acid;BUTTPARK 144\07-19;2-IODO-5-METHYLBENZOIC ACID;BERM-001
CAS:52548-14-8
MF:C8H7IO2
MW:262.04
EINECS:200-002-4
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Acids & Esters;Iodine Compounds
Mol File:52548-14-8.mol
2-IODO-5-METHYLBENZOIC ACID Structure
2-IODO-5-METHYLBENZOIC ACID Chemical Properties
Melting point 122-124°C
Boiling point 321.4±30.0 °C(Predicted)
density 1.867±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
form solid
pka2.93±0.10(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C8H7IO2/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4H,1H3,(H,10,11)
InChIKeyINGWGCDYAJKXKP-UHFFFAOYSA-N
SMILESC(O)(=O)C1=CC(C)=CC=C1I
CAS DataBase Reference52548-14-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
WGK Germany WGK 3
HazardClass LIGHT SENSITIVE
HS Code 2916399090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
2-IODO-5-METHYLBENZOIC ACID Usage And Synthesis
Chemical PropertiesWhite solid
Synthesis
m-Toluic acid

99-04-7

2-IODO-5-METHYLBENZOIC ACID

52548-14-8

Using 3-methylbenzoic acid (20 g, 0.15 mol) as raw material, the reaction was carried out according to the procedure of Example 1. Upon completion of the reaction, the conversion of 3-methylbenzoic acid was 50%. The products were isolated to give 1) 6-iodo-3-methylbenzoic acid in 40% yield and 2) other regional isomers of iodide in 8% yield. The ratio of product 1) to product 2) was 5:1.

References[1] ACS Catalysis, 2018, vol. 8, # 2, p. 920 - 925
[2] Patent: EP1595862, 2005, A1. Location in patent: Page/Page column 8
[3] Patent: EP1595862, 2005, A1. Location in patent: Page/Page column 8
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1974, p. 2405 - 2409
[5] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1973, p. 2940 - 2948
Tag:2-IODO-5-METHYLBENZOIC ACID(52548-14-8) Related Product Information
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