Ethyl 2-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

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Reagent Code: #184943
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CAS Number 1394003-51-0

science Other reagents with same CAS 1394003-51-0

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Weight 270.08 g/mol
Formula C₉H₈BrN₃O₂
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MDL Number MFCD22543888
inventory_2 Storage & Handling
Density 1.72±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anxiolytic drugs. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating compounds with central nervous system activity. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to its heterocyclic framework. Commonly utilized in research settings for generating novel bioactive molecules through cross-coupling and nucleophilic substitution reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,990.00
inventory 250mg
10-20 days ฿9,450.00
inventory 1g
10-20 days ฿36,690.00

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Ethyl 2-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anxiolytic drugs. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating compounds with central nervous system activity. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to its heterocyclic framework. Commonly utilized in research settings for generating novel bioactive molecules through c

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anxiolytic drugs. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating compounds with central nervous system activity. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to its heterocyclic framework. Commonly utilized in research settings for generating novel bioactive molecules through cross-coupling and nucleophilic substitution reactions.

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