7-Sulfamoyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide

Base Information

Chemical Name:7-Sulfamoyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide
CAS No.:23141-82-4
Molecular Formula:C₇H₉N₃O₄S₂
Molecular Weight:263.298
Hs Code.:
DSSTox Substance ID:DTXSID00879117
Nikkaji Number:J716.388F
Wikidata:Q82861166

Synonyms:23141-82-4;7-Sulfamoyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide;1,1-dioxo-3,4-dihydro-2H-1lambda6,2,4-benzothiadiazine-7-sulfonamide;hydrothiazide;Hydrochlorothiazide Impurity 4;SCHEMBL182359;DTXSID00879117;BCP33897;3,4-Dihydro-2H-benzo[e][1,2,4]thiadiazine-7-sulfonamide 1,1-dioxide;7-Sulfamoyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide;dihydro-2h-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide

Suppliers and Price of 7-Sulfamoyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide

Supply Marketing:

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

Total 5 raw suppliers

Chemical Property of 7-Sulfamoyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide

Chemical Property:

Melting Point:208-210 °C
Boiling Point:570.2±60.0 °C(Predicted)
Density:1.606±0.06 g/cm3(Predicted)
XLogP3:-0.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:1
Exact Mass:263.00344812
Heavy Atom Count:16
Complexity:461

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1NC2=C(C=C(C=C2)S(=O)(=O)N)S(=O)(=O)N1

Technology Process of 7-Sulfamoyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide

There total 1 articles about 7-Sulfamoyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide 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:

: 67-56-1
methanol

: 58-93-5,8049-49-8
6-chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide

: 121-30-2
chloraminophenamide

: 40642-90-8
4-amino-1,3-benzenedisulfonamide

: 4-Amino-6-hydroxy-benzene-1,3-disulfonic acid diamide

: 6-Hydroxy-1,1-dioxo-1,2,3,4-tetrahydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide

: 23141-82-4
3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide

: 32059-40-8
6-methoxy-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide

Guidance literature:: In water; Product distribution; Mechanism; Irradiation; multistep reaction, photholytic decomposition; also in pure MeOH; effect of O₂;
DOI:10.1002/jps.2600720221