(3-Chloro-4-(difluoromethoxy)pyridin-2-yl)methanamine hydrochloride

98%

Reagent Code: #131209
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CAS Number 2231674-65-8

science Other reagents with same CAS 2231674-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.05 g/mol
Formula C₇H₈Cl₂F₂N₂O
badge Registry Numbers
MDL Number MFCD31621181
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in drug design for oncology. Also utilized in agrochemical research for developing novel pesticides with improved environmental profiles. The amine functionality allows for easy derivatization, facilitating the creation of compound libraries for high-throughput screening in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,350.00
inventory 100mg
10-20 days ฿20,990.00

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(3-Chloro-4-(difluoromethoxy)pyridin-2-yl)methanamine hydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in drug design for oncology. Also utilized in agrochemical research for developing novel pesticides with improved environmental profiles. The amine functionality allows for easy derivatization, facilitating the creation of compound libraries for high-throughput screening

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in drug design for oncology. Also utilized in agrochemical research for developing novel pesticides with improved environmental profiles. The amine functionality allows for easy derivatization, facilitating the creation of compound libraries for high-throughput screening in medicinal chemistry.

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