Methyl 2-(2-chloroethoxy)acetate

97%

Reagent Code: #206088
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CAS Number 83881-47-4

science Other reagents with same CAS 83881-47-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.5760 g/mol
Formula C₅H₉ClO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves in the preparation of ethers and esters through alkylation reactions. Commonly employed in the development of active ingredients in plant growth regulators and herbicides. Also utilized in the synthesis of specialty polymers and functionalized solvents due to its reactive chloro and ester groups. Its bifunctional nature allows for sequential chemical modifications, making it valuable in multi-step synthesis routes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿143.00
1g
10-20 days ฿187.00
5g
10-20 days ฿764.50
25g
10-20 days ฿3,245.00
Methyl 2-(2-chloroethoxy)acetate
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves in the preparation of ethers and esters through alkylation reactions. Commonly employed in the development of active ingredients in plant growth regulators and herbicides. Also utilized in the synthesis of specialty polymers and functionalized solvents due to its reactive chloro and ester groups. Its bifunctional nature allows for sequential chemical modifications, making it valuab

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves in the preparation of ethers and esters through alkylation reactions. Commonly employed in the development of active ingredients in plant growth regulators and herbicides. Also utilized in the synthesis of specialty polymers and functionalized solvents due to its reactive chloro and ester groups. Its bifunctional nature allows for sequential chemical modifications, making it valuable in multi-step synthesis routes.

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