Methyl 4-amino-1,2,5-thiadiazole-3-carboxylate

97%

Reagent Code: #208886
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CAS Number 63875-18-3

science Other reagents with same CAS 63875-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.17 g/mol
Formula C₄H₅N₃O₂S
badge Registry Numbers
MDL Number MFCD01208070
thermostat Physical Properties
Boiling Point 267.8±20.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders and antimicrobial agents. Its structure supports the formation of biologically active heterocyclic compounds. Commonly employed in medicinal chemistry for constructing fused ring systems that enhance drug potency and selectivity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles. Serves as a building block in the preparation of fluorescent dyes and optical materials due to its electron-rich scaffold.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,330.00
inventory 250mg
10-20 days ฿2,120.00
inventory 1g
10-20 days ฿5,340.00
Methyl 4-amino-1,2,5-thiadiazole-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders and antimicrobial agents. Its structure supports the formation of biologically active heterocyclic compounds. Commonly employed in medicinal chemistry for constructing fused ring systems that enhance drug potency and selectivity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles. Serves as

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders and antimicrobial agents. Its structure supports the formation of biologically active heterocyclic compounds. Commonly employed in medicinal chemistry for constructing fused ring systems that enhance drug potency and selectivity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles. Serves as a building block in the preparation of fluorescent dyes and optical materials due to its electron-rich scaffold.

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