CAS 68292-02-4

Fórmula: C9H10N2O3S

InChI: InChI=1S/C9H10N2O3S/c1-10-15(12,13)6-8-7-4-2-3-5-9(7)14-11-8/h2-5,10H,6H2,1H3

Chave InChI: IFLCNEUQVNHBJU-UHFFFAOYSA-N

SMILES: CNS(=O)(=O)CC1=NOC2=CC=CC=C21

1-(Benzo[d]isoxazol-3-yl)-N-methylmethanesulfonamide

CAS: 68292-02-4

Pureza: 98%

Ref: IN-DA00FDJL

1-(Benzo[d]isoxazol-3-yl)-N-methylmethanesulfonamide

CAS: 68292-02-4

1-(Benzo[d]isoxazol-3-yl)-N-methylmethanesulfonamide

Fórmula: C₉H₁₀N₂O₃S

Pureza: 98%

Peso molecular: 226.26

Ref: 54-OR1061726

N-Methyl Zonisamide

CAS: 68292-02-4

Fórmula: C₉H₁₀N₂O₃S

Cor e Forma: White To Off-White Solid

Peso molecular: 226.25

Ref: 4Z-Z-034

1-(Benzo[d]isoxazol-3-yl)-N-methylmethanesulfonamide

CAS: 68292-02-4

1-(Benzo[d]isoxazol-3-yl)-N-methylmethanesulfonamide

Fórmula: C₉H₁₀N₂O₃S

Pureza: 98%

Peso molecular: 226.25

Ref: IN-DG01839029

N-Methyl zonisamide

CAS: 68292-02-4

N-Methyl zonisamide is a drug that is an impurity in Zonisamide. It is an analog of the drug and has been used as a research and development standard for Zonisamide. N-Methyl zonisamide can be synthesized from the corresponding nitrobenzene, aminobenzene, and formaldehyde. The synthesis can be performed by converting nitrobenzene to aminobenzene with sodium hydroxide in methanol, followed by conversion to N-methyl zonisamide with formaldehyde in ethanol. Pharmacopoeia standards for this compound are available from Sigma Aldrich, which can be purchased from our website.

Fórmula: C₉H₁₀N₂O₃S

Pureza: Min. 95 Area-%

Cor e Forma: Powder

Peso molecular: 226.25 g/mol

Ref: 3D-IM25576

N-Methyl Zonisamide

Produto Controlado

CAS: 68292-02-4

Applications A methylated analog of Zonisamide (Z700000) with anticonvulsant activity.
References Uno, H., et al.: J. Med. Chem., 22, 180 (1979)

Fórmula: C₉H₁₀N₂O₃S

Cor e Forma: Neat

Peso molecular: 226.25

Ref: TR-M338605

N-Methyl Zonisamide

CAS: 68292-02-4

Fórmula: C₉H₁₀N₂O₃S

Peso molecular: 226.3

Ref: ST-EA-CP-Z10001