2-Oxiranemethanol, 2-(4-methylbenzenesulfonate)

99%

Reagent Code: #221902
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CAS Number 6746-81-2

science Other reagents with same CAS 6746-81-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.26 g/mol
Formula C₁₀H₁₂O₄S
badge Registry Numbers
MDL Number MFCD00066850
thermostat Physical Properties
Boiling Point 95-100 ℃(Press:0.01Torr)
inventory_2 Storage & Handling
Density 1.310±0.06 g/cm3(Predicted)
Storage 2-8℃, dry

description Product Description

Used as a bifunctional reactive intermediate in organic synthesis, featuring both an epoxide ring and a tosylate leaving group. The epoxide functionality enables ring-opening reactions with nucleophiles such as amines, alcohols, or thiols, making it valuable in the preparation of epoxy-based polymers, crosslinking agents, specialty resins, coatings, and adhesives. The tosylate group facilitates efficient nucleophilic substitution, allowing the introduction of the glycidyl moiety into complex molecules. Commonly employed in pharmaceutical synthesis to build intricate frameworks, introduce hydroxymethyl groups, or modify biomolecules and polymers under mild conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿420.00
5g
10-20 days ฿3,360.00
25g
10-20 days ฿4,860.00
100g
10-20 days ฿17,781.50
2-Oxiranemethanol, 2-(4-methylbenzenesulfonate)
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Used as a bifunctional reactive intermediate in organic synthesis, featuring both an epoxide ring and a tosylate leaving group. The epoxide functionality enables ring-opening reactions with nucleophiles such as amines, alcohols, or thiols, making it valuable in the preparation of epoxy-based polymers, crosslinking agents, specialty resins, coatings, and adhesives. The tosylate group facilitates efficient nucleophilic substitution, allowing the introduction of the glycidyl moiety into complex molecules. Comm
Used as a bifunctional reactive intermediate in organic synthesis, featuring both an epoxide ring and a tosylate leaving group. The epoxide functionality enables ring-opening reactions with nucleophiles such as amines, alcohols, or thiols, making it valuable in the preparation of epoxy-based polymers, crosslinking agents, specialty resins, coatings, and adhesives. The tosylate group facilitates efficient nucleophilic substitution, allowing the introduction of the glycidyl moiety into complex molecules. Commonly employed in pharmaceutical synthesis to build intricate frameworks, introduce hydroxymethyl groups, or modify biomolecules and polymers under mild conditions.
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