4-chloro-7-methyl-2,3-dihydro-1H-indol-2-one

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Reagent Code: #195762
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CAS Number 943526-33-8

science Other reagents with same CAS 943526-33-8

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Weight 181.62 g/mol
Formula C₉H₈ClNO
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MDL Number MFCD21961280
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Storage Room temperature

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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. It serves as a building block in the development of small-molecule drugs due to its ability to bind selectively to ATP pockets in enzyme targets. Also explored in the design of anti-inflammatory and neuroprotective agents owing to its structural similarity to bioactive indole derivatives. Its derivatization enhances metabolic stability and blood-brain barrier penetration in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,900.00
inventory 250mg
10-20 days ฿24,000.00
inventory 1g
10-20 days ฿61,600.00

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4-chloro-7-methyl-2,3-dihydro-1H-indol-2-one
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. It serves as a building block in the development of small-molecule drugs due to its ability to bind selectively to ATP pockets in enzyme targets. Also explored in the design of anti-inflammatory and neuroprotective agents owing to its structural similarity to bioactive indole derivatives. Its derivatization enhances metabolic stability

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. It serves as a building block in the development of small-molecule drugs due to its ability to bind selectively to ATP pockets in enzyme targets. Also explored in the design of anti-inflammatory and neuroprotective agents owing to its structural similarity to bioactive indole derivatives. Its derivatization enhances metabolic stability and blood-brain barrier penetration in drug candidates.

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