2-(Methylamino)-1,3-thiazole-4-carboxylicacid

98%

Reagent Code: #213444
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CAS Number 1199216-02-8

science Other reagents with same CAS 1199216-02-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.18 g/mol
Formula C₅H₆N₂O₂S
badge Registry Numbers
MDL Number MFCD12785830
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in agrochemicals for creating novel pesticides and herbicides due to its stable heterocyclic structure. Also employed in research for designing enzyme inhibitors and bioactive molecules. Its functional groups allow easy modification for targeted molecular design in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,240.00
inventory 250mg
10-20 days ฿7,590.00
inventory 1g
10-20 days ฿15,250.00
inventory 5g
10-20 days ฿48,380.00
inventory 10g
10-20 days ฿67,700.00
2-(Methylamino)-1,3-thiazole-4-carboxylicacid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in agrochemicals for creating novel pesticides and herbicides due to its stable heterocyclic structure. Also employed in research for designing enzyme inhibitors and bioactive molecules. Its functional groups allow easy modification for targeted molecular design in drug discovery.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and anti-inflammatory properties. It serves as a building block in agrochemicals for creating novel pesticides and herbicides due to its stable heterocyclic structure. Also employed in research for designing enzyme inhibitors and bioactive molecules. Its functional groups allow easy modification for targeted molecular design in drug discovery.

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