Benzyl 2-chloroacetate

99 %

Reagent Code: #144917
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CAS Number 140-18-1

science Other reagents with same CAS 140-18-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.62 g/mol
Formula C₉H₉ClO₂
badge Registry Numbers
MDL Number MFCD00157062
thermostat Physical Properties
Boiling Point 90°C 1mm Hg (Lit.)
inventory_2 Storage & Handling
Density 1.2150 g/cm3
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a benzyl-protecting group reagent for alcohols and acids in multi-step synthesis. Commonly employed in the production of active pharmaceutical ingredients where selective protection and deprotection are required. Also utilized in the synthesis of ester derivatives and as a building block in the development of more complex organic molecules. Its reactivity allows for easy introduction of the chloroacetyl group, which can undergo further transformations such as nucleophilic substitution or cyclization reactions.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿860.00
inventory 100g
10-20 days ฿6,680.00
inventory 500g
10-20 days ฿24,120.00
inventory 25g
10-20 days ฿3,020.00

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Benzyl 2-chloroacetate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a benzyl-protecting group reagent for alcohols and acids in multi-step synthesis. Commonly employed in the production of active pharmaceutical ingredients where selective protection and deprotection are required. Also utilized in the synthesis of ester derivatives and as a building block in the development of more complex organic molecules. Its reactivity allows for easy introd

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a benzyl-protecting group reagent for alcohols and acids in multi-step synthesis. Commonly employed in the production of active pharmaceutical ingredients where selective protection and deprotection are required. Also utilized in the synthesis of ester derivatives and as a building block in the development of more complex organic molecules. Its reactivity allows for easy introduction of the chloroacetyl group, which can undergo further transformations such as nucleophilic substitution or cyclization reactions.

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