Ethyl 2-bromo-4-methylpentanoate

95%

Reagent Code: #130161
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CAS Number 35657-97-7

science Other reagents with same CAS 35657-97-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.11 g/mol
Formula C₈H₁₅BrO₂
badge Registry Numbers
MDL Number MFCD20483822
thermostat Physical Properties
Boiling Point 86-87 °C at 11 mmHg
inventory_2 Storage & Handling
Density 1.253±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. The ester group can be hydrolyzed to yield carboxylic acid derivatives or reduced to form alcohols, making it versatile in multi-step syntheses. Commonly employed in the development of active ingredients in crop protection agents and in the synthesis of bioactive compounds with potential therapeutic effects.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,530.00
250mg
10-20 days ฿9,390.00
1g
10-20 days ฿25,340.00
Ethyl 2-bromo-4-methylpentanoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. The ester group can be hydrolyzed to yield carboxylic acid derivatives or reduced to form alcohols, making it versatile in multi-step syntheses. Commonly employed in the development of active ingredients in crop protection agents and in the

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. The ester group can be hydrolyzed to yield carboxylic acid derivatives or reduced to form alcohols, making it versatile in multi-step syntheses. Commonly employed in the development of active ingredients in crop protection agents and in the synthesis of bioactive compounds with potential therapeutic effects.

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