N,2,4,6-tetramethylbenzenesulfonamide

Base Information

• Chemical Name: N,2,4,6-tetramethylbenzenesulfonamide
• CAS No.: 106003-69-4
• Molecular Formula: C10H15NO2S
• Molecular Weight: 213.301
• DSSTox Substance ID: DTXSID00355401
• Wikidata: Q82134280

Synonyms:N,2,4,6-tetramethylbenzenesulfonamide;106003-69-4;N,2,4,6-tetramethylbenzene-1-sulfonamide;Benzenesulfonamide, N,2,4,6-tetramethyl-;STK068182;SCHEMBL813077;DTXSID00355401;AKOS000427965;SB79284;CS-0235559;EN300-15852;AP-263/11633954;SR-01000325562;SR-01000325562-1;Z45527667;7KT

Chemical Property of N,2,4,6-tetramethylbenzenesulfonamide

Chemical Property:

• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 213.08234989
• Heavy Atom Count: 14
• Complexity: 269

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=C(C(=C1)C)S(=O)(=O)NC)C

Technology Process of N,2,4,6-tetramethylbenzenesulfonamide

There total 4 articles about N,2,4,6-tetramethylbenzenesulfonamide 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: 92.0%

2-mesitylenesulphonyl chloride (773-64-8) + methylamine (74-89-5) → 2,4,6-trimethyl-N-methylbenzenesulfonamide (106003-69-4)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Inert atmosphere; Schlenk technique;

DOI:10.1002/ejoc.202100955

Reference yield: 80.0%

bis(1-methyl-1-phenylethyl)peroxide (80-43-3) + 2,4,6-trimethylbenzenesulfonamide (4543-58-2) → 2,4,6-trimethyl-N-methylbenzenesulfonamide (106003-69-4)

Guidance literature:

With copper acetylacetonate; In acetone; at 120 ℃; for 8h; Sealed tube;

DOI:10.1080/00397911.2020.1859118

Reference yield:

2,4,6-trimethyl-benzenesulfonic acid-(methyl-nitroso-amide) (217497-19-3) + N-methylaniline (100-61-8) → 2,4,6-trimethyl-N-methylbenzenesulfonamide (106003-69-4) + N-methyl-N-nitrosoaniline (614-00-6)

Guidance literature:

In 1,4-dioxane; water; at 25 ℃; Rate constant;

DOI:10.1002/(SICI)1099-1395(1998100)11:10<756::AID-POC48>3.0.CO;2-D

upstream raw materials:

2-mesitylenesulphonyl chloride

methylamine

2,4,6-trimethyl-benzenesulfonic acid-(methyl-nitroso-amide)

N-methylaniline

Downstream raw materials:

2,4,6-trimethyl-benzenesulfonic acid-(methyl-nitroso-amide)

N-methyl-N'-(2,7-octadienyl)-2,4,6-trimethylbenzenesulfamide

C₂₄H₃₄N₂O₄S₂

C₂₅H₃₈N₂O₇S₃

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
  FOB CIF CFR EXW
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 106003-69-4 Benzenesulfonamide, N,2,4,6-tetramethyl-

Send

Send

Metric Ton KG G Pound L ML

Send

Send