4-iodo-2-Methylbenzoic acid

Base Information

• Chemical Name: 4-iodo-2-Methylbenzoic acid
• CAS No.: 133232-58-3
• Molecular Formula: C8H7IO2
• Molecular Weight: 262.047
• Hs Code.: 2916399090
• Mol file: 133232-58-3.mol

Synonyms:4-iodo-2-Methylbenzoic acid

Chemical Property of 4-iodo-2-Methylbenzoic acid

Chemical Property:

• Melting Point: 172 °C(Solv: water (7732-18-5))
• Boiling Point: 326.5±30.0 °C(Predicted)
• PKA: 3.70±0.25(Predicted)
• PSA: 37.30000
• Density: 1.867±0.06 g/cm3(Predicted)
• LogP: 2.29780
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility.: Aqueous Base (Slightly), Chloroform (Slightly), DMSO (Slightly)

Purity/Quality:

99%, ^*data from raw suppliers

5-IodotoluicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 5-Iodotoluic Acid can be used as 15-PGDH inhibitor to prevent and treat 15-PGDH-related diseases, for instance, fibrosis, inflammation, cardiovascular disease, wound, and auto-immune diseases.

Technology Process of 4-iodo-2-Methylbenzoic acid

There total 4 articles about 4-iodo-2-Methylbenzoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

2-methyl-4-iodoacetophenone (52164-27-9) → 4-iodo-2-methylbenzoic acid (133232-58-3)

Guidance literature:

With 1,4-dioxane; sodium hypobromide;

DOI:10.1246/bcsj.30.958

Reference yield:

→ 4-iodo-2-methylbenzoic acid (133232-58-3)

Guidance literature:

With potassium iodide;

Reference yield:

3-Iodotoluene (625-95-6) → 4-iodo-2-methylbenzoic acid (133232-58-3)

Guidance literature:

Multi-step reaction with 2 steps

1: AlCl₃

2: dioxane; aqueous NaBrO

With 1,4-dioxane; aluminium trichloride; sodium hypobromide;

upstream raw materials:

2-methyl-4-iodoacetophenone

3-Iodotoluene

Downstream raw materials:

4-iodo-2-methyl-benzoic acid methyl ester

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