Ethyl(6-Amino-1,2,3,4-Tetrahydro-1,3-Dimethyl-2,4-Dioxo-5-Pyrimidinyl)-Carbamate

95%

Reagent Code: #184367
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CAS Number 49810-21-1

science Other reagents with same CAS 49810-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.23 g/mol
Formula C₉H₁₄N₄O₄
badge Registry Numbers
MDL Number MFCD00192132
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of xanthine derivatives with potential bronchodilator and anti-asthmatic properties. It plays a role in the preparation of active compounds targeting respiratory diseases due to its structural similarity to methylxanthines. Also utilized in research settings for designing novel heterocyclic compounds with biological activity. Its carbamate and amino groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,990.00
inventory 500mg
10-20 days ฿6,780.00
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Ethyl(6-Amino-1,2,3,4-Tetrahydro-1,3-Dimethyl-2,4-Dioxo-5-Pyrimidinyl)-Carbamate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of xanthine derivatives with potential bronchodilator and anti-asthmatic properties. It plays a role in the preparation of active compounds targeting respiratory diseases due to its structural similarity to methylxanthines. Also utilized in research settings for designing novel heterocyclic compounds with biological activity. Its carbamate and amino groups allow for further chemical modifications, making it valua

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of xanthine derivatives with potential bronchodilator and anti-asthmatic properties. It plays a role in the preparation of active compounds targeting respiratory diseases due to its structural similarity to methylxanthines. Also utilized in research settings for designing novel heterocyclic compounds with biological activity. Its carbamate and amino groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug candidates.

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