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4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide
4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide
CAS No. 654-62-6
4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide( 4-Amino-6-(trifluoromethyl)benzene-1,3-d | 2,4-Disulfamyl-5-trifluoromethylaniline | 2-amino-4-trifluoromethyl-1,5-benzendisulfonamide )
Catalog No. M24666 CAS No. 654-62-6
4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide is a carbonic anhydrase inhibitor, used as a potential anti-tumor and antiglaucoma drug.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 46 | In Stock |
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| 5MG | 38 | In Stock |
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| 10MG | 57 | In Stock |
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| 25MG | 101 | In Stock |
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| 50MG | 147 | In Stock |
|
| 100MG | 212 | In Stock |
|
| 200MG | 318 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide
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NoteResearch use only, not for human use.
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Brief Description4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide is a carbonic anhydrase inhibitor, used as a potential anti-tumor and antiglaucoma drug.
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Description4-Amino-6-(trifluoromethyl)benzene-1,3-disulfonamide is a carbonic anhydrase inhibitor, used as a potential anti-tumor and antiglaucoma drug.
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In Vitro——
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In Vivo——
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Synonyms4-Amino-6-(trifluoromethyl)benzene-1,3-d | 2,4-Disulfamyl-5-trifluoromethylaniline | 2-amino-4-trifluoromethyl-1,5-benzendisulfonamide
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PathwayMembrane Transporter/Ion Channel
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TargetCarbonic Anhydrase
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Recptorcarbonic anhydrase
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Research Area——
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Indication——
Chemical Information
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CAS Number654-62-6
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Formula Weight319.28
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Molecular FormulaC7H8F3N3O4S2
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Purity>98% (HPLC)
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Solubility——
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SMILESNc(cc(C(F)(F)F)c(S(N)(=O)=O)c1)c1S(N)(=O)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Chohan ZH, Rauf A, Naseer MM, Somra MA, Supuran CT.Antibacterial, antifungal and cytotoxic properties of some sulfonamide-derived chromones.[J].J Enzyme Inhib Med Chem. 2006 Apr;21(2)
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