2-Bromo-2-methylbutane

95%

Reagent Code: #147406
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CAS Number 507-36-8

science Other reagents with same CAS 507-36-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.05 g/mol
Formula C₅H₁₁Br
badge Registry Numbers
MDL Number MFCD00000127
thermostat Physical Properties
Boiling Point 107°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as an alkylating agent in reactions where a bromine atom is displaced to form new carbon-carbon or carbon-heteroatom bonds. Commonly employed in laboratory settings for the preparation of Grignard reagents when reacted with magnesium in anhydrous ether. Also utilized in the synthesis of specialty polymers and functionalized hydrocarbons due to its reactivity in substitution and elimination reactions. Its branched structure makes it suitable for studying reaction mechanisms, particularly SN1 and SN2 pathways in educational and research contexts.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿720.00
inventory 5g
10-20 days ฿1,860.00
inventory 25g
10-20 days ฿7,710.00
inventory 100g
10-20 days ฿27,000.00
2-Bromo-2-methylbutane
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as an alkylating agent in reactions where a bromine atom is displaced to form new carbon-carbon or carbon-heteroatom bonds. Commonly employed in laboratory settings for the preparation of Grignard reagents when reacted with magnesium in anhydrous ether. Also utilized in the synthesis of specialty polymers and functionalized hydrocarbons due to its reactivity in substitution

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as an alkylating agent in reactions where a bromine atom is displaced to form new carbon-carbon or carbon-heteroatom bonds. Commonly employed in laboratory settings for the preparation of Grignard reagents when reacted with magnesium in anhydrous ether. Also utilized in the synthesis of specialty polymers and functionalized hydrocarbons due to its reactivity in substitution and elimination reactions. Its branched structure makes it suitable for studying reaction mechanisms, particularly SN1 and SN2 pathways in educational and research contexts.

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