Tetrahydro-2H-pyran-4-sulfonyl chloride

97%

Reagent Code: #242433
fingerprint
CAS Number 338453-21-7

science Other reagents with same CAS 338453-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.64 g/mol
Formula C₆H₉ClO₃S
badge Registry Numbers
MDL Number MFCD07787616
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a sulfonating agent in organic synthesis, enabling the introduction of sulfonyl groups to alcohols, amines, and other nucleophiles. Its reactivity makes it valuable for creating sulfonate esters and sulfonamides, which serve as intermediates in pharmaceuticals and agrochemicals. The tetrahydro-2H-pyran-4-sulfonyl group acts as a protecting group modifier due to its stability under various reaction conditions and ease of removal when needed. Commonly employed in multi-step syntheses where selective functionalization is required, especially in the development of active pharmaceutical ingredients (APIs). Handling requires caution due to its moisture sensitivity and potential for exothermic reactions with nucleophiles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿759.00
inventory 250mg
10-20 days ฿1,331.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Tetrahydro-2H-pyran-4-sulfonyl chloride
No image available

Used primarily as a sulfonating agent in organic synthesis, enabling the introduction of sulfonyl groups to alcohols, amines, and other nucleophiles. Its reactivity makes it valuable for creating sulfonate esters and sulfonamides, which serve as intermediates in pharmaceuticals and agrochemicals. The tetrahydro-2H-pyran-4-sulfonyl group acts as a protecting group modifier due to its stability under various reaction conditions and ease of removal when needed. Commonly employed in multi-step syntheses wher

Used primarily as a sulfonating agent in organic synthesis, enabling the introduction of sulfonyl groups to alcohols, amines, and other nucleophiles. Its reactivity makes it valuable for creating sulfonate esters and sulfonamides, which serve as intermediates in pharmaceuticals and agrochemicals. The tetrahydro-2H-pyran-4-sulfonyl group acts as a protecting group modifier due to its stability under various reaction conditions and ease of removal when needed. Commonly employed in multi-step syntheses where selective functionalization is required, especially in the development of active pharmaceutical ingredients (APIs). Handling requires caution due to its moisture sensitivity and potential for exothermic reactions with nucleophiles.

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...