(Methylsulfamoyl)amine

Base Information

• Chemical Name: (Methylsulfamoyl)amine
• CAS No.: 72179-84-1
• Molecular Formula: CH6N2O2S
• Molecular Weight: 110.137
• European Community (EC) Number: 850-251-2
• DSSTox Substance ID: DTXSID30524325
• Nikkaji Number: J2.189.652G
• Wikidata: Q82391107
• Mol file: 72179-84-1.mol

Synonyms:(methylsulfamoyl)amine;N-methylsulfamide;72179-84-1;(sulfamoylamino)methane;methyl sulfamide;Sulfamide, methyl-;MFCD02691960;methylsulfamide;methyl(sulfamoyl)amine;N-Methylsulfuric diamide;SCHEMBL20211;DTXSID30524325;NOXPGSDFQWSNSW-UHFFFAOYSA-N;AKOS000167618;PB43354;BS-12662;SY020910;CS-0035488;EN300-50354;F20082;Z56762361;F8880-1261

Chemical Property of (Methylsulfamoyl)amine

Chemical Property:

• Melting Point: 65.5-66.0 °C
• Boiling Point: 229.0±23.0 °C(Predicted)
• PKA: 11.67±0.60(Predicted)
• PSA: 80.57000
• Density: 1.401±0.06 g/cm3(Predicted)
• LogP: 0.58130
• Water Solubility.: 溶于水
• XLogP3: -1.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 110.01499861
• Heavy Atom Count: 6
• Complexity: 108

Purity/Quality:

99%, ^*data from raw suppliers

N-Methylsulfamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNS(=O)(=O)N
• Uses: N-Methylsulfamide is a useful synthetic compound. N-Methylsulfamide is a derivative of Sulfamide (S699079) which is a carbonic anhydrase inhibitor, used for treatment of cancer.

Technology Process of (Methylsulfamoyl)amine

There total 5 articles about (Methylsulfamoyl)amine 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:

N-(tert-butoxycarbonyl)-N'-(methyl)sulfamide (125987-94-2) → N-methylsulfamide (72179-84-1)

Guidance literature:

N-(tert-butoxycarbonyl)-N'-(methyl)sulfamide; With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃;

With sodium hydrogencarbonate; In water; ethyl acetate;

DOI:10.1016/j.tetasy.2013.04.006

Reference yield:

N-methylsulfamoyl chloride (10438-96-7) → N-methylsulfamide (72179-84-1)

Guidance literature:

With ammonia; In toluene;

Reference yield:

methyl-μ-imido-disulfuric acid diamide (4047-86-3) → N-methylsulfamide (72179-84-1)

Guidance literature:

With water;

upstream raw materials:

methyl-μ-imido-disulfuric acid diamide

methylamine

N-methylsulfamoyl chloride

N-(tert-butoxycarbonyl)-N'-(methyl)sulfamide

Downstream raw materials:

(+/-)-8-cyclohexyl-5-[[[(methylamino)sulfonyl]amino]carbonyl]-1,2b-dihydro-11-methoxy-cycloprop[d]indolo[2,1-a][2]benzazepine-1a(2H)-carboxylic acid methyl ester

N-(n-methylsulfamoyl)benzamide

4-cyano-N-(n-methylsulfamoyl)benzamide

N-methyl-N'-[phenylmethylidene]sulfamide

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