Isopropyl methanesulfonate

97%

Reagent Code: #199777
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CAS Number 926-06-7

science Other reagents with same CAS 926-06-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.19 g/mol
Formula C₄H₁₀O₃S
thermostat Physical Properties
Melting Point 5.5-6.5°C
Boiling Point 82°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an alkylating agent in organic synthesis, enabling the introduction of isopropyl groups to various substrates. It is particularly effective in the preparation of pharmaceutical intermediates and fine chemicals due to its reactivity with nucleophiles such as amines, alcohols, and thiols. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where selective alkylation is required. Its use is favored in certain reactions due to the good leaving group ability of the methanesulfonate moiety, facilitating efficient substitution under mild conditions. Handling requires caution due to its potential toxicity and alkylating properties, which may pose mutagenic or carcinogenic risks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿280.00
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿450.00
inventory 25g
10-20 days ฿1,990.00
inventory 100g
10-20 days ฿7,150.00
inventory 500g
10-20 days ฿27,540.00
Isopropyl methanesulfonate
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Used primarily as an alkylating agent in organic synthesis, enabling the introduction of isopropyl groups to various substrates. It is particularly effective in the preparation of pharmaceutical intermediates and fine chemicals due to its reactivity with nucleophiles such as amines, alcohols, and thiols. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where selective alkylation is required. Its use is favored in certain reactions due to the good leaving group ability of the

Used primarily as an alkylating agent in organic synthesis, enabling the introduction of isopropyl groups to various substrates. It is particularly effective in the preparation of pharmaceutical intermediates and fine chemicals due to its reactivity with nucleophiles such as amines, alcohols, and thiols. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where selective alkylation is required. Its use is favored in certain reactions due to the good leaving group ability of the methanesulfonate moiety, facilitating efficient substitution under mild conditions. Handling requires caution due to its potential toxicity and alkylating properties, which may pose mutagenic or carcinogenic risks.

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