Ethyl 3-amino-3-iminopropanoate

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Reagent Code: #184202
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CAS Number 50551-10-5

science Other reagents with same CAS 50551-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.15 g/mol
Formula C₆H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD06797615
thermostat Physical Properties
Boiling Point 197.1 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-alanine derivatives and other biologically active compounds. It serves in the development of drugs targeting neurological and cardiovascular conditions due to its ability to act as a building block for heterocyclic structures. Also employed in agrochemical formulations for enhancing the stability and reactivity of active ingredients. Its amino-imino tautomerism makes it valuable in coordination chemistry for designing metal-organic frameworks and catalysts.

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inventory 1g
10-20 days ฿9,600.00

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Ethyl 3-amino-3-iminopropanoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-alanine derivatives and other biologically active compounds. It serves in the development of drugs targeting neurological and cardiovascular conditions due to its ability to act as a building block for heterocyclic structures. Also employed in agrochemical formulations for enhancing the stability and reactivity of active ingredients. Its amino-imino tautomerism makes it valuable in coordination chemistr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-alanine derivatives and other biologically active compounds. It serves in the development of drugs targeting neurological and cardiovascular conditions due to its ability to act as a building block for heterocyclic structures. Also employed in agrochemical formulations for enhancing the stability and reactivity of active ingredients. Its amino-imino tautomerism makes it valuable in coordination chemistry for designing metal-organic frameworks and catalysts.

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