4-Iodo-3-methoxybenzaldehyde

Base Information

• Chemical Name: 4-Iodo-3-methoxybenzaldehyde
• CAS No.: 121404-83-9
• Molecular Formula: C8H7IO2
• Molecular Weight: 262.047
• Hs Code.: 2912490090
• European Community (EC) Number: 828-920-5
• Mol file: 121404-83-9.mol

Synonyms:4-IODO-3-METHOXYBENZALDEHYDE;121404-83-9;MFCD11847312;4-Iodo-3-methoxy-benzaldehyde;SCHEMBL432936;PHSPBXTVMJOTQN-UHFFFAOYSA-N;WEA40483;AKOS022178307;CS-11734;SY028995;CS-0083460;A1-11970

Chemical Property of 4-Iodo-3-methoxybenzaldehyde

Chemical Property:

• PSA: 26.30000
• LogP: 2.11230
• Storage Temp.: 2-8°C
• XLogP3: 2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 261.94908
• Heavy Atom Count: 11
• Complexity: 138

Purity/Quality:

97% ^*data from raw suppliers

4-Iodo-3-methoxybenzaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=CC(=C1)C=O)I

Technology Process of 4-Iodo-3-methoxybenzaldehyde

There total 8 articles about 4-Iodo-3-methoxybenzaldehyde 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: 97.0%

3-hydroxy-4-iodobenzaldehyde (135242-71-6) + methyl iodide (74-88-4) → 4-iodo-3-methoxybenzaldehyde (121404-83-9)

Guidance literature:

With potassium carbonate; In acetone; for 2h; Heating / reflux;

Reference yield: 95.0%

(4-iodo-3-methoxyphenyl)methanol → 4-iodo-3-methoxybenzaldehyde (121404-83-9)

Guidance literature:

With manganese(IV) oxide; In chloroform; for 16h; Reflux; Inert atmosphere; Industrial scale;

Reference yield: 66.0%

3-methoxy-benzaldehyde (591-31-1) → 2-iodo-5-methoxybenzaldehyde (77287-58-2) + 4-iodo-3-methoxybenzaldehyde (121404-83-9)

Guidance literature:

With 1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione; 1,3-bis(3,5-bis(trifluoro-ethyl)phenyl)thiourea; In acetonitrile; at 20 ℃; regioselective reaction; Schlenk technique; Inert atmosphere;

DOI:10.1055/s-0033-1338468

upstream raw materials:

methyl iodide

3-hydroxy-4-iodobenzaldehyde

methyl 4-iodo-3-methoxybenzoate

methyl 3-methoxy-4-aminobenzoate

Downstream raw materials:

4-iodo-3-(2-iodo-5-methoxybenzoyloxy)benzaldehyde

2-(4-iodo-3-methoxy-phenyl)-5,5-dimethyl-[1,3]dioxane

C₁₇H₂₂ClIO₃

3-methoxy-4-(2-methylpyridin-4-yl)benzaldehyde

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