Ethyl chlorodifluoroacetate

98%

Reagent Code: #181557
label
Alias Ethyl difluoroacetate
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CAS Number 383-62-0

science Other reagents with same CAS 383-62-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.53 g/mol
Formula C₄H₅ClF₂O₂
badge Registry Numbers
EC Number 206-850-0
MDL Number MFCD00013662
thermostat Physical Properties
Boiling Point 96-97.5 °C(lit.)
inventory_2 Storage & Handling
Density 1.252 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the introduction of difluoromethyl groups into organic molecules. It serves in the preparation of fluorinated building blocks for drug development due to its ability to participate in nucleophilic substitution and esterification reactions. Commonly employed in the manufacture of non-steroidal anti-inflammatory drugs (NSAIDs) and certain herbicides, where the fluorine atoms enhance metabolic stability and bioavailability. Also utilized in research laboratories for the development of novel fluorinated compounds with tailored biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿320.00
25g
10-20 days ฿1,000.00
100g
10-20 days ฿3,490.00
500g
10-20 days ฿17,020.00
Ethyl chlorodifluoroacetate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the introduction of difluoromethyl groups into organic molecules. It serves in the preparation of fluorinated building blocks for drug development due to its ability to participate in nucleophilic substitution and esterification reactions. Commonly employed in the manufacture of non-steroidal anti-inflammatory drugs (NSAIDs) and certain herbicides, where the fluorine atoms enhance metabolic stability and bio

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the introduction of difluoromethyl groups into organic molecules. It serves in the preparation of fluorinated building blocks for drug development due to its ability to participate in nucleophilic substitution and esterification reactions. Commonly employed in the manufacture of non-steroidal anti-inflammatory drugs (NSAIDs) and certain herbicides, where the fluorine atoms enhance metabolic stability and bioavailability. Also utilized in research laboratories for the development of novel fluorinated compounds with tailored biological activity.

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