(2-Aminophenyl)methanesulfonamide

Base Information

• Chemical Name: (2-Aminophenyl)methanesulfonamide
• CAS No.: 344750-18-1
• Molecular Formula: C₇H₁₀N₂O₂S
• Molecular Weight: 186.235
• European Community (EC) Number: 853-500-3

Synonyms:(2-aminophenyl)methanesulfonamide;344750-18-1;(2-Amino-phenyl)-methanesulfonamide;SCHEMBL449211;AKOS010113932;EN300-130084;G22929

Chemical Property of (2-Aminophenyl)methanesulfonamide

Chemical Property:

• XLogP3: -0.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 186.04629874
• Heavy Atom Count: 12
• Complexity: 232

Purity/Quality:

(2-AMINOPHENYL)METHANESULFONAMIDE 95 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)CS(=O)(=O)N)N

Technology Process of (2-Aminophenyl)methanesulfonamide

There total 2 articles about (2-Aminophenyl)methanesulfonamide 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-nitrophenylmethanesulfonamide (51145-00-7) → (2-amino-phenyl)-methanesulfonic acid amide (344750-18-1)

Guidance literature:

With palladium on activated charcoal; ethanol;

DOI:10.1021/ja01527a044

Reference yield:

2-nitrobenzylsulfonyl chloride (24974-75-2) → (2-amino-phenyl)-methanesulfonic acid amide (344750-18-1)

Guidance literature:

Multi-step reaction with 2 steps

1: NH₃

2: iron

With ammonia; iron;

DOI:10.1021/ja01527a044

Reference yield:

(2-amino-phenyl)-methanesulfonic acid amide (344750-18-1) → C7H8N3O2S(1+)*BF4(1-)

Guidance literature:

With tetrafluoroboric acid; sodium nitrite; In water; at 0 - 5 ℃; for 1.5h;

DOI:10.1002/jps.2600730321

upstream raw materials:

2-nitrophenylmethanesulfonamide

2-nitrobenzylsulfonyl chloride

Downstream raw materials:

(2-amino-5-bromo-phenyl)-methanesulfonic acid amide

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