5-(2-Methyl-1,3-thiazol-4-yl)-3-isoxazolecarboxylic acid

97%

Reagent Code: #214401
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CAS Number 368870-05-7

science Other reagents with same CAS 368870-05-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.21 g/mol
Formula C₈H₆N₂O₃S
badge Registry Numbers
MDL Number MFCD03086107
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. It serves as a building block in medicinal chemistry due to its heterocyclic structure, which enhances binding affinity to biological targets. Also applied in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its functional groups allow for easy modification, making it valuable in high-throughput screening and structure-activity relationship studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿21,200.00
5-(2-Methyl-1,3-thiazol-4-yl)-3-isoxazolecarboxylic acid
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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. It serves as a building block in medicinal chemistry due to its heterocyclic structure, which enhances binding affinity to biological targets. Also applied in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its functional groups allow for easy modification, making it valuable in high-throughput screening and structure

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its heterocyclic structure, which enhances binding affinity to biological targets. Also applied in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its functional groups allow for easy modification, making it valuable in high-throughput screening and structure-activity relationship studies.

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