Ethyl 3-[4-Amino-2-(methylthio)-5-thiazolyl]-3-oxopropanoate

≥95%

Reagent Code: #185713
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CAS Number 65095-75-2

science Other reagents with same CAS 65095-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.33 g/mol
Formula C₉H₁₂N₂O₃S₂
badge Registry Numbers
MDL Number MFCD03068914
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as an intermediate in the synthesis of thiamine (vitamin B1), this compound plays a key role in pharmaceutical and fine chemical manufacturing. Its functional groups enable selective reactions for building complex heterocyclic systems. It is particularly valuable in producing bioactive molecules and analogs used in nutritional supplements and medicinal chemistry. The methylthio and amino-thiazole moieties contribute to its reactivity in condensation and coupling reactions, making it suitable for developing compounds with biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,900.00
inventory 1g
10-20 days ฿15,000.00
inventory 5g
10-20 days ฿37,500.00

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Ethyl 3-[4-Amino-2-(methylthio)-5-thiazolyl]-3-oxopropanoate
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Used as an intermediate in the synthesis of thiamine (vitamin B1), this compound plays a key role in pharmaceutical and fine chemical manufacturing. Its functional groups enable selective reactions for building complex heterocyclic systems. It is particularly valuable in producing bioactive molecules and analogs used in nutritional supplements and medicinal chemistry. The methylthio and amino-thiazole moieties contribute to its reactivity in condensation and coupling reactions, making it suitable for dev

Used as an intermediate in the synthesis of thiamine (vitamin B1), this compound plays a key role in pharmaceutical and fine chemical manufacturing. Its functional groups enable selective reactions for building complex heterocyclic systems. It is particularly valuable in producing bioactive molecules and analogs used in nutritional supplements and medicinal chemistry. The methylthio and amino-thiazole moieties contribute to its reactivity in condensation and coupling reactions, making it suitable for developing compounds with biological activity.

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