7-bromo-5-methyl-1H-indazole

≥95%

Reagent Code: #194087
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CAS Number 885272-97-9

science Other reagents with same CAS 885272-97-9

blur_circular Chemical Specifications

product.molecular_weight - string(6) "211.06"

product.molecular_formula - string(14) "C₈H₇BrN₂"

scatter_plot Molecular Information
Weight 211.06 g/mol
Formula C₈H₇BrN₂
product.einec_s_num - string(0) ""

product.mdl_num - string(12) "MFCD05664004"

badge Registry Numbers
MDL Number MFCD05664004
product.melting_point - string(0) ""

product.boiling_point - string(0) ""

product.density - string(0) ""

product.storage_conditions - string(16) "Room temperature"

inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in pharmaceutical research and development as an intermediate in the synthesis of biologically active compounds. It serves as a building block in the creation of kinase inhibitors, which are important in the study of cancer and inflammatory diseases. Its indazole core structure is valued for its ability to interact with various enzyme targets, making it useful in the design of new drug candidates. Additionally, it has been explored in the development of compounds targeting neurological pathways due to its structural similarity to known neuroactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿830.00
inventory 250mg
10-20 days ฿1,460.00
inventory 1g
10-20 days ฿4,050.00

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7-bromo-5-methyl-1H-indazole
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Used primarily in pharmaceutical research and development as an intermediate in the synthesis of biologically active compounds. It serves as a building block in the creation of kinase inhibitors, which are important in the study of cancer and inflammatory diseases. Its indazole core structure is valued for its ability to interact with various enzyme targets, making it useful in the design of new drug candidates. Additionally, it has been explored in the development of compounds targeting neurological pathways due to its structural similarity to known neuroactive molecules.
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