4-hydroxy-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide

Base Information

Chemical Name:4-hydroxy-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide
CAS No.:141233-20-7
Molecular Formula:C10H10N2O4S
Molecular Weight:254.266
Hs Code.:
DSSTox Substance ID:DTXSID80435735
Nikkaji Number:J3.192.948B
Wikidata:Q82250821
ChEMBL ID:CHEMBL27248

Synonyms:141233-20-7;CHEMBL27248;4-Hydroxy-N-(5-methylisoxazol-3-yl)benzenesulfonamide;4-hydroxy-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide;DTXSID80435735;BDBM50034414;4-Hydroxy-N-(5-methyl-isoxazol-3-yl)-benzenesulfonamide;4-Hydroxy-N-(5-methylisoxazole-3-yl)benzene-1-sulfonamide

Suppliers and Price of 4-hydroxy-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 4-hydroxy-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:254.03612798
Heavy Atom Count:17
Complexity:346

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=NO1)NS(=O)(=O)C2=CC=C(C=C2)O

Technology Process of 4-hydroxy-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide

There total 4 articles about 4-hydroxy-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide 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: 69.0%

: 723-46-6
sulfamethoxazole

: 141233-20-7
4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide

Guidance literature:: sulfamethoxazole; With tetrafluoroboric acid; In water; at 20 ℃; for 0.0333333h;

With sodium nitrite; In water; at 0 ℃; for 0.5h;

With copper(I) oxide; copper(II) sulfate; In water; at 0 - 20 ℃; for 0.5h;
DOI:10.1080/00397911.2018.1496263

Reference yield: 41.0%

: 4-methoxy-N-(5-methylisoxazol-3-yl)benzenesulfonamide

: 141233-20-7
4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide

Guidance literature:: With boron tribromide; In dichloromethane; at -78 - 20 ℃; for 5.5h; Inert atmosphere;
DOI:10.1021/tx500267x

Reference yield:

: 723-46-6
sulfamethoxazole

: 1072-67-9
5-methylisoxazol-3-ylamine

: 98-10-2
benzenesulfonamide

: 533-73-3
1,2,4-Trihydroxybenzene

: 547-44-4
N-((4-aminophenyl)sulfonyl)carbamimidic acid

: 20759-40-4
3-hydroxybenzenesulfonamide

: 4-amino-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

: N-(4,5-dihydroxy-5-methyl-4,5-dihydroisoxazol-3-yl)-4-hydroxybenzenesulfonamide

: N-(4,5-dihydroxy-5-methyl-4,5-dihydroisoxazol-3-yl)benzenesulfonamide

: (Z)-N-((2-oxopropylidene)carbamoyl)methanesulfonamide

: 3,4-dihydroxy-N-(5-methylisoxazol-3-yl)benzenesulfonamide

: 3,4-dihydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

: 4-amino-3-hydroxy-N- (5-methylisoxazol-3-yl)benzenesulfonamide

: 4-amino-3-hydroxy-N-(4-hydroxy-5-methylisoxazol-3-yl)benzenesulfonamide

: 2-oxo-N-(phenylsulfonyl)acetimidamide

: 141233-20-7
4-hydroxy-N-(5-methyl-3-isoxazolyl)benzenesulphonamide

: 29699-89-6
N-(5-methyl-isoxazol-3-yl)-4-nitro-benzenesulfonamide

: 108-95-2,27073-41-2
phenol

Guidance literature:: With AgBr-BaMoO₄ composite photocatalyst; In water; for 1.25h; Reagent/catalyst; Kinetics; UV-irradiation;
DOI:10.1016/j.jphotochem.2018.07.007