2-Isopropyl-5-methylcyclohexyl 2-chloroacetate

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Reagent Code: #201206
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CAS Number 106916-72-7

science Other reagents with same CAS 106916-72-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.75 g/mol
Formula C₁₂H₂₁ClO₂
badge Registry Numbers
MDL Number MFCD00040700
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure allows for selective reactions in the development of chiral compounds, making it valuable in the production of certain pesticides and bioactive molecules. The presence of both ester and chloroacetate functionalities enables further chemical modifications, facilitating its role in multi-step organic syntheses. It is also employed in research settings for exploring reaction mechanisms involving nucleophilic substitution and ester hydrolysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,560.00
inventory 250mg
10-20 days ฿2,760.00
inventory 1g
10-20 days ฿8,670.00
inventory 5g
10-20 days ฿30,320.00

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2-Isopropyl-5-methylcyclohexyl 2-chloroacetate
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Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure allows for selective reactions in the development of chiral compounds, making it valuable in the production of certain pesticides and bioactive molecules. The presence of both ester and chloroacetate functionalities enables further chemical modifications, facilitating its role in multi-step organic syntheses. It is also employed in research settings for exploring reaction mechanisms involving nucleophil

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure allows for selective reactions in the development of chiral compounds, making it valuable in the production of certain pesticides and bioactive molecules. The presence of both ester and chloroacetate functionalities enables further chemical modifications, facilitating its role in multi-step organic syntheses. It is also employed in research settings for exploring reaction mechanisms involving nucleophilic substitution and ester hydrolysis.

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