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Sulfamide

Base Information Edit
  • Chemical Name:Sulfamide
  • CAS No.:7803-58-9
  • Molecular Formula:H4N2O2S
  • Molecular Weight:96.11
  • Hs Code.:28530090
  • European Community (EC) Number:232-262-9
  • NSC Number:252
  • UNII:VS7TZW634V
  • DSSTox Substance ID:DTXSID5064885
  • Nikkaji Number:J134.318A
  • Wikipedia:Sulfamide
  • Wikidata:Q3048282
  • Pharos Ligand ID:KL5DSHS1MS5D
  • ChEMBL ID:CHEMBL355001
  • Mol file:7803-58-9.mol
Sulfamide

Synonyms:Sulfamide;Sulfuric diamide;7803-58-9;Sulfamamide;Sulfuryl amide;sulphamide;Sulfonyl diamide;Sulfuryl diamide;sulfamoylamine;Sulphuric diamide;H4N2O2S;Imidosulfamic acid;MFCD00011606;Imidosulfamic acid (VAN);H2NSO2NH2;UNII-VS7TZW634V;VS7TZW634V;CHEMBL355001;CHEBI:29368;NSC 252;NSC-252;EINECS 232-262-9;AI3-30237;Sulfuricdiamide;aminosulfonamide;diamidodioxidosulfur;Sulfamide, 99%;SULFAMIDE [MI];NH2SO2NH2;NSC252;DTXSID5064885;BDBM26995;H4-N2-O2-S;[S(NH2)2O2];BCP13844;STR07407;BBL019229;S O2 (N H2)2;STK505662;Sulfamide, purum, >=99.0% (N);AKOS000201755;CCG-266025;CS-W013732;s12311;SY004124;BB 0260582;FT-0601025;S5606;A839317;Q-201768;Q3048282;Z104503438;FUS

Suppliers and Price of Sulfamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Sulfamide
  • 100mg
  • $ 403.00
  • Usbiological
  • Sulfamide
  • 100g
  • $ 333.00
  • TRC
  • Sulfamide
  • 5g
  • $ 90.00
  • TCI Chemical
  • Sulfamide >96.0%(N)
  • 25g
  • $ 25.00
  • TCI Chemical
  • Sulfamide >96.0%(N)
  • 250g
  • $ 122.00
  • SynQuest Laboratories
  • Sulfamide 98%
  • 500 g
  • $ 184.00
  • SynQuest Laboratories
  • Sulfamide 98%
  • 100 g
  • $ 61.00
  • Sigma-Aldrich
  • Sulfamide purum, ≥99.0% (N)
  • 50g
  • $ 341.00
  • Sigma-Aldrich
  • Sulfamide 99%
  • 25g
  • $ 43.00
  • Sigma-Aldrich
  • Sulfamide 99%
  • 5g
  • $ 102.00
Total 168 raw suppliers
Chemical Property of Sulfamide Edit
Chemical Property:
  • Appearance/Colour:White solid 
  • Melting Point:90-92 °C(lit.) 
  • Refractive Index:1.548 
  • PKA:10.87±0.60(Predicted) 
  • PSA:94.56000 
  • Density:1.688 g/cm3 
  • LogP:0.63000 
  • Storage Temp.:Refrigerator 
  • Sensitive.:Moisture Sensitive 
  • Solubility.:water: soluble50mg/mL, clear, colorless to faintly yellow 
  • Water Solubility.:soluble 
  • XLogP3:-1.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:95.99934855
  • Heavy Atom Count:5
  • Complexity:85.3
Purity/Quality:

98% *data from raw suppliers

Sulfamide *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36-37/39 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:NS(=O)(=O)N
  • Description Sulfamide is a white solid substance that is normally produced by reacting sulfuryl chloride with ammonia. Sulfamide is stable under normal conditions and soluble in acetone and DMSO. Sulfamide may also refer to the functional group in organic chemistry, and it consists of at least one group attached to a nitrogen atom of sulfamide. It is a carbonic anhydrase inhibitor and is widely used as a pharmaceutical intermediate. Sulfamide is sensitive to moisture, thus should be kept away from water and humidity. It should also be stored away from oxidizing agents. Sulfamide should be kept in a tightly closed container and placed in a cool, dry, and well-ventilated condition.
  • Uses Similar to urea in many of its reactions, but is more acidic, and can act as a dibasic acid. A carbonic anhydrase inhibitor; used for treatment of cancer. Sulfamide and its derivatives can also be used to prepare fused thiadiazine systems, Reaction with 2-aminoacetophenones affords IH-2,1,3-benzothia- diazine 2,2-dioxides 77 (65JOC3960). The corresponding 3,4-dihydro deriv- atives are readily available from 2-aminobenzylamines with either sulfuryl chloride (70M1443) or sulfamide (66USP3278532; 71MI055). These kinds of compounds can also be obtained from N-aryl-N'-alkylsulfamides and s-trioxane in a reaction involving cyclization by intramolecular sulfamido- methylation (79JOC2032) (Scheme 30).
Technology Process of Sulfamide

There total 46 articles about Sulfamide 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:
Guidance literature:
In Petroleum ether; addn. of SO2Cl2 in dry petroleum ether to liquid NH3 (cooling: solid CO2 in CHCl3/CCl4); removal of cooling (removal of excess NH3); decanting of solvent; warming; - further information (to diminish vehemence of reaction) given;; extraction (soxhlet/CH3COOCH3); evapn.; drying (vac.); recrystn. from water; further information (extraction/increase of yield) given;;
Guidance literature:
With water; heat of evapn., 2 h, 2 M HCl;
Guidance literature:
With water; in the cold, 48 h, 2 M HCl;
Refernces Edit
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