2-(2-Bromo-5-methoxyphenyl)propan-2-ol

98%

Reagent Code: #130152
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CAS Number 853271-15-5

science Other reagents with same CAS 853271-15-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.11 g/mol
Formula C₁₀H₁₃BrO₂
badge Registry Numbers
MDL Number MFCD28125772
thermostat Physical Properties
Melting Point 96.8-97.8 °C(Solv: ethyl ether (60-29-7))
Boiling Point 310.9±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.382±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and analgesic agents. Its structure allows for selective modification to enhance bioavailability and receptor binding in central nervous system drugs. Also employed in research for developing novel serotonin receptor modulators due to the presence of methoxy and bromo substituents on the aromatic ring, which influence binding affinity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,440.00
inventory 250mg
10-20 days ฿14,330.00
inventory 1g
10-20 days ฿38,700.00

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2-(2-Bromo-5-methoxyphenyl)propan-2-ol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and analgesic agents. Its structure allows for selective modification to enhance bioavailability and receptor binding in central nervous system drugs. Also employed in research for developing novel serotonin receptor modulators due to the presence of methoxy and bromo substituents on the aromatic ring, which influence binding affinity and metabolic stability.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and analgesic agents. Its structure allows for selective modification to enhance bioavailability and receptor binding in central nervous system drugs. Also employed in research for developing novel serotonin receptor modulators due to the presence of methoxy and bromo substituents on the aromatic ring, which influence binding affinity and metabolic stability.

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