4H-1,2,4-Benzothiadiazine-3-butanoic acid 1,1-dioxide

Base Information

Chemical Name:4H-1,2,4-Benzothiadiazine-3-butanoic acid 1,1-dioxide
CAS No.:4826-24-8
Molecular Formula:C₁₁H₁₂N₂O₄S
Molecular Weight:268.293
Hs Code.:
Mol file:4826-24-8.mol

Synonyms:3-(3-Carboxypropyl)-4H-1,2,4-benzothiadiazine 1,1-dioxide;4H-1,2,4-Benzothiadiazine-3-butanoic acid 1,1-dioxide

Suppliers and Price of 4H-1,2,4-Benzothiadiazine-3-butanoic acid 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 0 raw suppliers

Chemical Property of 4H-1,2,4-Benzothiadiazine-3-butanoic acid 1,1-dioxide

Chemical Property:

PSA：104.21000
LogP:2.10860

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4H-1,2,4-Benzothiadiazine-3-butanoic acid 1,1-dioxide

There total 4 articles about 4H-1,2,4-Benzothiadiazine-3-butanoic acid 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: 81.0%

: 4-(2-Sulfamoyl-phenylcarbamoyl)-butyric acid methyl ester

: 4826-24-8
1,2,4-Benzothiadiazin-1,1-dioxid-3-butansaeure

Guidance literature:: With sodium hydroxide; for 0.166667h;
DOI:10.1002/ardp.19853181008

Reference yield:

: 1501-26-4
methyl 4-(chlorocarbonyl)butyrate

: 4826-24-8
1,2,4-Benzothiadiazin-1,1-dioxid-3-butansaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / N,N-dimethyl-acetamide / 20 - 25 °C

2: 81 percent / 4percent aq. NaOH / 0.17 h

With sodium hydroxide; In N,N-dimethyl acetamide;
DOI:10.1002/ardp.19853181008

Reference yield:

: 3306-62-5
2-AMINOBENZENESULFONAMIDE

: 4826-24-8
1,2,4-Benzothiadiazin-1,1-dioxid-3-butansaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / N,N-dimethyl-acetamide / 20 - 25 °C

2: 81 percent / 4percent aq. NaOH / 0.17 h

With sodium hydroxide; In N,N-dimethyl acetamide;
DOI:10.1002/ardp.19853181008