Ethyl 5-amino-1-(2,5-difluorophenyl)pyrazole-4-carboxylate

98%

Reagent Code: #185049
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CAS Number 138907-69-4

science Other reagents with same CAS 138907-69-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.236 g/mol
Formula C₁₂H₁₁F₂N₃O₂
badge Registry Numbers
MDL Number MFCD06795943
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in creating targeted therapies. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies due to its stable pyrazole core and functional groups that allow further derivatization.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,420.00
Ethyl 5-amino-1-(2,5-difluorophenyl)pyrazole-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in creating targeted therapies. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies due to its stable pyrazole core and function

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in creating targeted therapies. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies due to its stable pyrazole core and functional groups that allow further derivatization.

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