3,4-Dihydroisoquinoline-2(1H)-sulfonyl chloride

95%

Reagent Code: #43956
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CAS Number 195987-27-0

science Other reagents with same CAS 195987-27-0

blur_circular Chemical Specifications

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Weight 231.6992 g/mol
Formula C₉H₁₀ClNO₂S
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MDL Number MFCD08443056
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound is valuable for introducing the 3,4-dihydroisoquinoline moiety into more complex molecules. It is commonly employed in the preparation of pharmaceuticals, particularly in the development of compounds with potential therapeutic effects on the central nervous system. Additionally, it serves as a key building block in the synthesis of sulfonamide derivatives, which are widely explored for their antibacterial and enzyme inhibitory properties. Its sulfonyl chloride group makes it highly reactive, facilitating efficient coupling reactions with amines or alcohols to form sulfonamides or sulfonate esters, respectively. This versatility makes it a useful tool in medicinal chemistry and drug discovery research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,546.00

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3,4-Dihydroisoquinoline-2(1H)-sulfonyl chloride
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Used primarily as a reactive intermediate in organic synthesis, this compound is valuable for introducing the 3,4-dihydroisoquinoline moiety into more complex molecules. It is commonly employed in the preparation of pharmaceuticals, particularly in the development of compounds with potential therapeutic effects on the central nervous system. Additionally, it serves as a key building block in the synthesis of sulfonamide derivatives, which are widely explored for their antibacterial and enzyme inhibitory

Used primarily as a reactive intermediate in organic synthesis, this compound is valuable for introducing the 3,4-dihydroisoquinoline moiety into more complex molecules. It is commonly employed in the preparation of pharmaceuticals, particularly in the development of compounds with potential therapeutic effects on the central nervous system. Additionally, it serves as a key building block in the synthesis of sulfonamide derivatives, which are widely explored for their antibacterial and enzyme inhibitory properties. Its sulfonyl chloride group makes it highly reactive, facilitating efficient coupling reactions with amines or alcohols to form sulfonamides or sulfonate esters, respectively. This versatility makes it a useful tool in medicinal chemistry and drug discovery research.

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