6-Bromo-8-methylthioimidazo[1,2-a]pyrazinamine

≥97%

Reagent Code: #151314
fingerprint
CAS Number 887475-71-0

science Other reagents with same CAS 887475-71-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.11 g/mol
Formula C₇H₆BrN₃S
badge Registry Numbers
MDL Number MFCD11100003
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting protein kinases involved in cancer cell proliferation. Shows potential in developing treatments for neurological disorders due to its ability to cross the blood-brain barrier. Also employed in the design of selective probes for studying enzyme activity in cellular systems. Its bromo and amine functional groups allow for further chemical modifications, making it valuable in structure-activity relationship (SAR) studies during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,930.00
inventory 1g
10-20 days ฿15,860.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Bromo-8-methylthioimidazo[1,2-a]pyrazinamine
No image available

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting protein kinases involved in cancer cell proliferation. Shows potential in developing treatments for neurological disorders due to its ability to cross the blood-brain barrier. Also employed in the design of selective probes for studying enzyme activity in cellular systems. Its bromo and amine functional groups allow for further chemical modifications, making it valuable in structure-act

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting protein kinases involved in cancer cell proliferation. Shows potential in developing treatments for neurological disorders due to its ability to cross the blood-brain barrier. Also employed in the design of selective probes for studying enzyme activity in cellular systems. Its bromo and amine functional groups allow for further chemical modifications, making it valuable in structure-activity relationship (SAR) studies during drug discovery.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...