3-SULFOLENE

98%

Reagent Code: #234705
label
Alias Butadiene sulfone; 3-thiophene dioxide; cyclobutyl sulfone; 3-sulfone cyclopentene; sulfonelenene
fingerprint
CAS Number 77-79-2

science Other reagents with same CAS 77-79-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 118.15 g/mol
Formula C₄H₆O₂S
badge Registry Numbers
MDL Number MFCD00005481
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as a precursor in organic synthesis, particularly as a masked source of 1,3-butadiene. It participates in Diels-Alder reactions, where it thermally decomposes upon heating to release butadiene and sulfur dioxide, enabling cycloaddition processes with dienophiles. This makes it valuable in the synthesis of cyclic compounds, including natural products and pharmaceuticals. It is also employed in the preparation of sulfone-containing molecules, which are important in medicinal chemistry and materials science due to their stability and electronic properties. Its role as a safe, solid alternative to gaseous butadiene enhances handling and storage in laboratory and industrial settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,000.00
inventory 100g
10-20 days ฿2,290.00
inventory 500g
10-20 days ฿9,540.00
inventory 2.5kg
10-20 days ฿43,990.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-SULFOLENE
No image available

Used primarily as a precursor in organic synthesis, particularly as a masked source of 1,3-butadiene. It participates in Diels-Alder reactions, where it thermally decomposes upon heating to release butadiene and sulfur dioxide, enabling cycloaddition processes with dienophiles. This makes it valuable in the synthesis of cyclic compounds, including natural products and pharmaceuticals. It is also employed in the preparation of sulfone-containing molecules, which are important in medicinal chemistry and ma

Used primarily as a precursor in organic synthesis, particularly as a masked source of 1,3-butadiene. It participates in Diels-Alder reactions, where it thermally decomposes upon heating to release butadiene and sulfur dioxide, enabling cycloaddition processes with dienophiles. This makes it valuable in the synthesis of cyclic compounds, including natural products and pharmaceuticals. It is also employed in the preparation of sulfone-containing molecules, which are important in medicinal chemistry and materials science due to their stability and electronic properties. Its role as a safe, solid alternative to gaseous butadiene enhances handling and storage in laboratory and industrial settings.

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...