1,1'-Sulfonyldiimidazole

97%

Reagent Code: #234603
label
Alias N,N'-sulfanyldiimidazole
fingerprint
CAS Number 7189-69-7

science Other reagents with same CAS 7189-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.2 g/mol
Formula C₆H₆N₄O₂S
badge Registry Numbers
EC Number 230-554-0
MDL Number MFCD00015893
thermostat Physical Properties
Melting Point 135-137 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly for the introduction of sulfonyl groups. It reacts with alcohols to form sulfonate esters, which are good leaving groups in substitution reactions. Also employed in the preparation of sulfonamides by reacting with amines, making it valuable in pharmaceutical synthesis. Its imidazole leaving group enhances reactivity under mild conditions, offering high selectivity. Useful in peptide chemistry and polymer modification due to low toxicity and ease of handling compared to other sulfonylating agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿350.00
inventory 25g
10-20 days ฿1,410.00
inventory 500g
10-20 days ฿24,980.00
inventory 1kg
10-20 days ฿46,620.00
inventory 2.5kg
10-20 days ฿108,870.00
inventory 100g
10-20 days ฿5,180.00
1,1'-Sulfonyldiimidazole
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Used as a reagent in organic synthesis, particularly for the introduction of sulfonyl groups. It reacts with alcohols to form sulfonate esters, which are good leaving groups in substitution reactions. Also employed in the preparation of sulfonamides by reacting with amines, making it valuable in pharmaceutical synthesis. Its imidazole leaving group enhances reactivity under mild conditions, offering high selectivity. Useful in peptide chemistry and polymer modification due to low toxicity and ease of han

Used as a reagent in organic synthesis, particularly for the introduction of sulfonyl groups. It reacts with alcohols to form sulfonate esters, which are good leaving groups in substitution reactions. Also employed in the preparation of sulfonamides by reacting with amines, making it valuable in pharmaceutical synthesis. Its imidazole leaving group enhances reactivity under mild conditions, offering high selectivity. Useful in peptide chemistry and polymer modification due to low toxicity and ease of handling compared to other sulfonylating agents.

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