(R)-2-Chloro-7-ethyl-8-isopropyl-7,8-dihydropteridin-6(5H)-one

95%

Reagent Code: #230447
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CAS Number 889877-77-4

science Other reagents with same CAS 889877-77-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.72 g/mol
Formula C₁₁H₁₅ClN₄O
badge Registry Numbers
MDL Number MFCD16620521
thermostat Physical Properties
Boiling Point 465.668°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of biologically active pteridine derivatives, particularly in the development of kinase inhibitors and antiviral agents. Its chiral chloro-keto structure allows selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in asymmetric synthesis to introduce the 7,8-dihydropteridinone scaffold with high stereocontrol, which is relevant in drug discovery programs targeting inflammatory diseases and certain cancers.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿650.00
inventory 1g
10-20 days ฿1,960.00
inventory 5g
10-20 days ฿5,760.00

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(R)-2-Chloro-7-ethyl-8-isopropyl-7,8-dihydropteridin-6(5H)-one
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Used as a key intermediate in the synthesis of biologically active pteridine derivatives, particularly in the development of kinase inhibitors and antiviral agents. Its chiral chloro-keto structure allows selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in asymmetric synthesis to introduce the 7,8-dihydropteridinone scaffold with high stereocontrol, which is relevant in drug discovery programs targeting inflammatory di

Used as a key intermediate in the synthesis of biologically active pteridine derivatives, particularly in the development of kinase inhibitors and antiviral agents. Its chiral chloro-keto structure allows selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in asymmetric synthesis to introduce the 7,8-dihydropteridinone scaffold with high stereocontrol, which is relevant in drug discovery programs targeting inflammatory diseases and certain cancers.

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