3-Chloro-4-morpholino-1,2,5-thiadiazole

98%

Reagent Code: #159758
label
Alias 4-(4-chloro-1,2,5-thiadiazole-3-yl)-morpholine; 3-morpholine-4-chloro-1,2,5-thiadiazole
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CAS Number 30165-96-9

science Other reagents with same CAS 30165-96-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.67 g/mol
Formula C₆H₈ClN₃OS
badge Registry Numbers
EC Number 250-077-1
thermostat Physical Properties
Melting Point 44-47 °C
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that enhance binding affinity with biological targets. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its reactivity allows for functionalization at multiple sites, making it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿204.00
inventory 25g
10-20 days ฿1,330.00
inventory 100g
10-20 days ฿4,480.00

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3-Chloro-4-morpholino-1,2,5-thiadiazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that enhance binding affinity with biological targets. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its reactivity allows for functionalization at multiple sites, making it valuable in

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that enhance binding affinity with biological targets. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its reactivity allows for functionalization at multiple sites, making it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

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