4-Methyl-5-(methylthio)thiazol-2-amine

95%

Reagent Code: #203460
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CAS Number 34006-41-2

science Other reagents with same CAS 34006-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.26 g/mol
Formula C₅H₈N₂S₂
badge Registry Numbers
MDL Number MFCD09938994
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of thiamine (vitamin B1), this compound plays an essential role in pharmaceutical manufacturing. It contributes to the construction of the thiazole ring system found in thiamine, enabling large-scale production of the vitamin for dietary supplements and fortification of foods. Its reactivity allows for efficient coupling with pyrimidine derivatives in vitamin B1 synthesis. Additionally, it serves in research settings for developing new bioactive molecules and heterocyclic compounds with potential therapeutic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,350.00
inventory 100mg
10-20 days ฿14,190.00
inventory 250mg
10-20 days ฿24,120.00
4-Methyl-5-(methylthio)thiazol-2-amine
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Used as a key intermediate in the synthesis of thiamine (vitamin B1), this compound plays an essential role in pharmaceutical manufacturing. It contributes to the construction of the thiazole ring system found in thiamine, enabling large-scale production of the vitamin for dietary supplements and fortification of foods. Its reactivity allows for efficient coupling with pyrimidine derivatives in vitamin B1 synthesis. Additionally, it serves in research settings for developing new bioactive molecules and h

Used as a key intermediate in the synthesis of thiamine (vitamin B1), this compound plays an essential role in pharmaceutical manufacturing. It contributes to the construction of the thiazole ring system found in thiamine, enabling large-scale production of the vitamin for dietary supplements and fortification of foods. Its reactivity allows for efficient coupling with pyrimidine derivatives in vitamin B1 synthesis. Additionally, it serves in research settings for developing new bioactive molecules and heterocyclic compounds with potential therapeutic properties.

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