
CAS Number127-69-5
Synonyms4-Amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide; 4-Amino-N-(3,4-dimethylisoxazol-5-yl)-benzenesulfonamide; 4-Amino-N-(3,4-dimethylisoxazol-5-yl)benzenesulfonamide; Gantrizin; Sulfisoxazole; T5NOJ CMSWR DZ& D1 E1; N1-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide; Sulfafurazole; EINECS 204-858-9; MFCD00003150; 4-Amino-N-(3,4-d; 5-(p-Aminobenzenesulfonamido)-3,4-dimethylisooxazole; 4-Amino-N-(3,4-dimethyl-1,2-oxazol-5-yl)benzenesulfonamide
Molecular FormulaC11H13N3O3S
Molecular Weight267.30
Purity98.00%
Density1.4±0.1 g/cm3
Boiling Point482.2±55.0 °C at 760 mmHg
Melting Point195°C
AppearanceWhite to cream powder
EINECS204-858-9
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 127-69-5 |
| Catalog No. | 2A-9020591 |
| Chinese Name | 磺胺二甲异唑 |
| Synonyms | 4-Amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide; 4-Amino-N-(3,4-dimethylisoxazol-5-yl)-benzenesulfonamide; 4-Amino-N-(3,4-dimethylisoxazol-5-yl)benzenesulfonamide; Gantrizin; Sulfisoxazole; T5NOJ CMSWR DZ& D1 E1; N1-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide; Sulfafurazole; EINECS 204-858-9; MFCD00003150; 4-Amino-N-(3,4-d; 5-(p-Aminobenzenesulfonamido)-3,4-dimethylisooxazole; 4-Amino-N-(3,4-dimethyl-1,2-oxazol-5-yl)benzenesulfonamide |
| Molecular Formula | C11H13N3O3S |
| Molecular Weight | 267.30 |
| Purity | 98.00 |
| Density | 1.4±0.1 g/cm3 |
| Boiling Point | 482.2±55.0 °C at 760 mmHg |
| Melting Point | 195°C |
| Appearance | White to cream powder |
| Water Solubility | <0.1 g/100 mL at 22.5 ºC |
| Storage Condition | 2-8°C |
| Application | Sulfisoxazole is an endothelin receptor antagonist and a sulfa antibiotic. |
| EINECS | 204-858-9 |
| HTC | 2935009090 |
| PubChem ID | 329753912 |
| MDL Number | MFCD00003150 |
| SMILES | Cc1noc(NS(=O)(=O)c2ccc(N)cc2)c1C |
| InChI | 1S/C11H13N3O3S/c1-7-8(2)13-17-11(7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6,14H,12H2,1-2H3 |
| InChI Key | NHUHCSRWZMLRLA-UHFFFAOYSA-N |
| Beilstein/REAXYS | 6737262 |
| NACRES Code | NA.24 |
| UNSPSC | 41116107 |
| Hazard Symbols | Transport |
| MSDS | msds/20591_1_127_69_5.pdf |
| Bioactivity | Sulfisoxazole, an endothelin receptor antagonist, is a sulfonamide antibacterial with an oxazole substituent.Target: Antibacterial; Endothelin ReceptorThe sulfanilamide antibacterial agent sulfisoxazole was found to be a good endothelin receptor antagonist (IC50's of 0.60 microM and 22 microM for the ETA and ETB receptors, respectively) [1]. Sulfisoxazole is used to treat or prevent infections in many different parts of the body. It belongs to the group of medicines known as sulfonamide antibiotics. It works by preventing the growth of bacteria [2]. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Signaling Pathways >> GPCR/G Protein >> Endothelin Receptor Research Areas >> Infection References [1]. Chan, M.F., et al., Identification of a new class of ETA selective endothelin antagonists by pharmacophore directed screening. Biochem Biophys Res Commun, 1994. 201(1): p. 228-34. [2]. http://www.mayoclinic.org/drugs-supplements/sulfisoxazole-oral-route/description/drg-20072998 Chemical & Physical Properties Density 1.4±0.1 g/cm3 Boiling Point 482.2±55.0 °C at 760 mmHg Melting Point 195°C Molecular Formula C11H13N3O3S Molecular Weight 267.304 Flash Point 245.4±31.5 °C Exact Mass 267.067749 PSA 106.60000 LogP 1.01 Vapour Pressure 0.0±1.2 mmHg at 25°C Index of Refraction 1.626 InChIKey NHUHCSRWZMLRLA-UHFFFAOYSA-N SMILES Cc1noc(NS(=O)(=O)c2ccc(N)cc2)c1C Storage condition 2-8°C Stability Stable. Incompatible with strong oxidizing agents. Water Solubility <0.1 g/100 mL at 22.5 ºC |
| Use of | Properties Articles52 Name sulfisoxazole Synonym More Synonyms Sulfisoxazole Biological Activity Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Signaling Pathways >> GPCR/G Protein >> Endothelin Receptor Research Areas >> Infection References [1]. Chan, M.F., et al., Identification of a new class of ETA selective endothelin antagonists by pharmacophore directed screening. Biochem Biophys Res Commun, 1994. 201(1): p. 228-34. [2]. http://www.mayoclinic.org/drugs-supplements/sulfisoxazole-oral-route/description/drg-20072998 Chemical & Physical Properties Molecular Formula C11H13N3O3S Exact Mass 267.067749 PSA 106.60000 Index of Refraction 1.626 InChIKey NHUHCSRWZMLRLA-UHFFFAOYSA-N Stability Stable. Incompatible with strong oxidizing agents. |
| Tax Rebate | 9.0% |
| Supervision | None MFN tariff: 6.5% Ordinary tariff: 35.0% |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available See reverse side of invoice or packing slip. |
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