2-Chloro-N,N-dimethylpyridin-4-amine

95%

Reagent Code: #163506
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CAS Number 59047-70-0

science Other reagents with same CAS 59047-70-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.61 g/mol
Formula C₇H₉ClN₂
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MDL Number MFCD09031034
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of herbicides and fungicides due to its ability to enhance bioavailability and stability in active compounds. Also employed in research settings for the preparation of novel heterocyclic compounds with potential biological activity. Its reactivity allows for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,810.00
inventory 250mg
10-20 days ฿9,620.00
inventory 1g
10-20 days ฿24,040.00

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2-Chloro-N,N-dimethylpyridin-4-amine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of herbicides and fungicides due to its ability to enhance bioavailability and stability in active compounds. Also employed in research settings for the preparation of novel heterocyclic compounds with potential biological activity. Its reactivity allows for easy functionalization, making it val

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of herbicides and fungicides due to its ability to enhance bioavailability and stability in active compounds. Also employed in research settings for the preparation of novel heterocyclic compounds with potential biological activity. Its reactivity allows for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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