acetamide, 2-chloro-N-[4-[[(3,4-dimethyl-5-isoxazolyl)amin

Base Information

Chemical Name:acetamide, 2-chloro-N-[4-[[(3,4-dimethyl-5-isoxazolyl)amin
CAS No.:104246-33-5
Molecular Formula:C₁₃H₁₄ClN₃O₄S
Molecular Weight:343.791
Hs Code.:
Mol file:104246-33-5.mol

Synonyms:2-chloro-N-[4-(3,4-dimethyl-isoxazol-5-ylsulfamoyl)-phenyl]-acetamide

Suppliers and Price of acetamide, 2-chloro-N-[4-[[(3,4-dimethyl-5-isoxazolyl)amin

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

Matrix Scientific
2-Chloro-N-(4-{[(3,4-dimethylisoxazol-5-yl)amino]-sulfonyl}phenyl)acetamide
500mg
$ 237.00

Crysdot
2-Chloro-N-(4-(N-(3,4-dimethylisoxazol-5-yl)sulfamoyl)phenyl)acetamide 97%
5g
$ 752.00

Total 5 raw suppliers

Chemical Property of acetamide, 2-chloro-N-[4-[[(3,4-dimethyl-5-isoxazolyl)amin

Chemical Property:

Purity/Quality:

97% ^*data from raw suppliers

2-Chloro-N-(4-{[(3,4-dimethylisoxazol-5-yl)amino]-sulfonyl}phenyl)acetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of acetamide, 2-chloro-N-[4-[[(3,4-dimethyl-5-isoxazolyl)amin

There total 1 articles about acetamide, 2-chloro-N-[4-[[(3,4-dimethyl-5-isoxazolyl)amin 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: 43.0%

: 127-69-5
sulfisoxazole

: 79-04-9
chloroacetyl chloride

: 104246-33-5
2-chloro-N-[4-(3,4-dimethyl-isoxazol-5-ylsulfamoyl)-phenyl]-acetamide

Guidance literature:: With triethylamine; In acetone; at 20 ℃; Cooling with ice;
DOI:10.2174/1573406415666190401144053

Reference yield: 32.0%

: 1453-82-3
isonicotinamide

: 104246-33-5
2-chloro-N-[4-(3,4-dimethyl-isoxazol-5-ylsulfamoyl)-phenyl]-acetamide

: 4-carbamoyl-1-{[4-(3,4-dimethyl-isoxazol-5-ylsulfamoyl)-phenylcarbamoyl]-methyl}-pyridinium chloride

Guidance literature:: In neat (no solvent); at 155 ℃; for 0.25h;
DOI:10.2174/1573406415666190401144053

Reference yield:

: 104246-33-5
2-chloro-N-[4-(3,4-dimethyl-isoxazol-5-ylsulfamoyl)-phenyl]-acetamide

: 1449513-62-5
N₄-[2-(4-fluorophenyl)-3-chloro-4-oxoazetidin-1-yl]aminoacetylamino-N₁-(3,4-dimethyl-1,2-oxazol-5-yl)benzensulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / ethanol / 10 h / Heating

2: acetic acid / ethanol / 8 h / Reflux

3: triethylamine / 1,4-dioxane / 8 h / 0 °C / Reflux

With hydrazine hydrate; acetic acid; triethylamine; In 1,4-dioxane; ethanol;
DOI:10.3390/molecules18044140