N-(3-Aminopropyl)cyclopropanesulfonamidehydrochloride

95%

Reagent Code: #220502
fingerprint
CAS Number 2253638-50-3

science Other reagents with same CAS 2253638-50-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.71 g/mol
Formula C₆H₁₅ClN₂O₂S
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block for gamma-aminobutyric acid (GABA) analogs due to its structural similarity to neurotransmitter molecules. Employed in the development of anticonvulsant and anxiolytic agents. Also utilized in research for designing enzyme inhibitors and receptor modulators. Its sulfonamide group enhances binding affinity in certain drug-receptor interactions, making it valuable in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,310.00
inventory 250mg
10-20 days ฿2,170.00
inventory 1g
10-20 days ฿4,350.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(3-Aminopropyl)cyclopropanesulfonamidehydrochloride
No image available

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block for gamma-aminobutyric acid (GABA) analogs due to its structural similarity to neurotransmitter molecules. Employed in the development of anticonvulsant and anxiolytic agents. Also utilized in research for designing enzyme inhibitors and receptor modulators. Its sulfonamide group enhances binding affinity in certain drug-recep

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block for gamma-aminobutyric acid (GABA) analogs due to its structural similarity to neurotransmitter molecules. Employed in the development of anticonvulsant and anxiolytic agents. Also utilized in research for designing enzyme inhibitors and receptor modulators. Its sulfonamide group enhances binding affinity in certain drug-receptor interactions, making it valuable in medicinal chemistry.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...