2-(5-Amino-2-methylanilino)-4-(3-pyridyl)pyrimidine

98%

Reagent Code: #134986
label
Alias N-(5-amino o-toluyl)-4-(3-pyridinyl)-2-pyrimidinyl; N-(5-amino-2-methylphenyl)-4-(3-pyridinyl)-2-aminopyrimidin; 4-methyl-N3-[4-(3-pyridinyl)-2-pyrimidinyl]-1,3-phenylenediamine
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CAS Number 152460-10-1

science Other reagents with same CAS 152460-10-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.33 g/mol
Formula C₁₆H₁₅N₅
badge Registry Numbers
MDL Number MFCD09028125
inventory_2 Storage & Handling
Storage -20°C

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 targeted therapies due to its ability to interact with specific enzyme pathways involved in tumor growth. Also employed in research settings for designing novel compounds with potential anti-inflammatory and antiviral properties. Its structural features make it valuable in medicinal chemistry for optimizing drug potency and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿132.00
inventory 5g
10-20 days ฿144.00
inventory 25g
10-20 days ฿380.00
inventory 100g
10-20 days ฿744.00
inventory 500g
10-20 days ฿6,130.00
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2-(5-Amino-2-methylanilino)-4-(3-pyridyl)pyrimidine
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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 targeted therapies due to its ability to interact with specific enzyme pathways involved in tumor growth. Also employed in research settings for designing novel compounds with potential anti-inflammatory and antiviral properties. Its structural features make it valuable in medicinal chemistry for optimizing drug potency and selec

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 targeted therapies due to its ability to interact with specific enzyme pathways involved in tumor growth. Also employed in research settings for designing novel compounds with potential anti-inflammatory and antiviral properties. Its structural features make it valuable in medicinal chemistry for optimizing drug potency and selectivity.

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