Ethyl 3-amino-3-oxopropanoate

98%

Reagent Code: #182380
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CAS Number 7597-56-0

science Other reagents with same CAS 7597-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.13 g/mol
Formula C₅H₉NO₃
thermostat Physical Properties
Melting Point 47-50°C
Boiling Point 265.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the production of pyrazoles and other nitrogen-containing rings. Commonly applied in pharmaceutical manufacturing for building active pharmaceutical ingredients (APIs), especially in antipyretic and analgesic drug classes. Also utilized in agrochemical synthesis for developing herbicides and plant growth regulators. Its bifunctional nature—bearing both amino and ester groups—makes it valuable in condensation reactions and peptide-like chain extensions in organic chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿168.00
25g
10-20 days ฿4,500.00
100g
10-20 days ฿18,000.00
5g
10-20 days ฿1,150.00
Ethyl 3-amino-3-oxopropanoate
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Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the production of pyrazoles and other nitrogen-containing rings. Commonly applied in pharmaceutical manufacturing for building active pharmaceutical ingredients (APIs), especially in antipyretic and analgesic drug classes. Also utilized in agrochemical synthesis for developing herbicides and plant growth regulators. Its bifunctional nature—bearing both amino and ester groups—makes it valuable in condensation reactions

Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the production of pyrazoles and other nitrogen-containing rings. Commonly applied in pharmaceutical manufacturing for building active pharmaceutical ingredients (APIs), especially in antipyretic and analgesic drug classes. Also utilized in agrochemical synthesis for developing herbicides and plant growth regulators. Its bifunctional nature—bearing both amino and ester groups—makes it valuable in condensation reactions and peptide-like chain extensions in organic chemistry.

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