4-Methylnaphthalene-1-sulfonamide

Base Information

• Chemical Name: 4-Methylnaphthalene-1-sulfonamide
• CAS No.: 10447-10-6
• Molecular Formula: C₁₁H₁₁NO₂S
• Molecular Weight: 221.28
• European Community (EC) Number: 840-802-5

Synonyms:4-methylnaphthalene-1-sulfonamide;10447-10-6;SCHEMBL2649239;4-methyl-1-naphthalenesulfonamide;MFCD09881050;AKOS013757448;SB79646;DS-19090;4-methyl-naphthalene-1-sulfonic acid amide;CS-0061330;C11167;EN300-276830;A906871;AQ-390/42850131

Chemical Property of 4-Methylnaphthalene-1-sulfonamide

Chemical Property:

• Melting Point: 175 °C
• Boiling Point: 426.6±38.0 °C(Predicted)
• Density: 1.311±0.06 g/cm3(Predicted)
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 221.05104977
• Heavy Atom Count: 15
• Complexity: 320

Purity/Quality:

97% ^*data from raw suppliers

4-Methylnaphthalene-1-sulfonamide 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1=CC=C(C2=CC=CC=C12)S(=O)(=O)N

Technology Process of 4-Methylnaphthalene-1-sulfonamide

There total 3 articles about 4-Methylnaphthalene-1-sulfonamide 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:

4-methyl-1-naphthalenesulfonyl chloride (10447-11-7) → 4-Methylnaphthalene-1-sulfonamide (10447-10-6)

Guidance literature:

In dichloromethane;

Reference yield:

→ 4-Methylnaphthalene-1-sulfonamide (10447-10-6)

Guidance literature:

With ammonia; water;

Reference yield:

4-Methyl-1-(trimethylstannyl)naphthalene (127686-17-3) → 4-Methylnaphthalene-1-sulfonamide (10447-10-6)

Guidance literature:

With isocyanate de chlorosulfonyle; Methamphetamin; Yield given. Multistep reaction; 1) CH₂Cl₂, 15 h, 20 deg C 2) 30 min;

upstream raw materials:

4-Methyl-1-(trimethylstannyl)naphthalene

4-methyl-1-naphthalenesulfonyl chloride

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