(2-Bromo-6-methylphenyl)methanol

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Reagent Code: #132673
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CAS Number 1055969-07-7

science Other reagents with same CAS 1055969-07-7

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Weight 201.06 g/mol
Formula C₈H₉BrO
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MDL Number MFCD16877028
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of active ingredients that require substituted benzyl moieties. Its bromo and hydroxyl functional groups allow for selective transformations, enabling coupling reactions or further derivatization through etherification, esterification, or cross-coupling processes. Commonly employed in research and development of new drug candidates, especially in routes involving bromoaryl building blocks for Suzuki or Ullmann-type reactions. Also utilized in the production of specialty chemicals where controlled substitution patterns on aromatic rings are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,550.00
inventory 1g
10-20 days ฿23,110.00

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(2-Bromo-6-methylphenyl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of active ingredients that require substituted benzyl moieties. Its bromo and hydroxyl functional groups allow for selective transformations, enabling coupling reactions or further derivatization through etherification, esterification, or cross-coupling processes. Commonly employed in research and development of new drug candidates, especially in routes involving bromoaryl building blocks for

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of active ingredients that require substituted benzyl moieties. Its bromo and hydroxyl functional groups allow for selective transformations, enabling coupling reactions or further derivatization through etherification, esterification, or cross-coupling processes. Commonly employed in research and development of new drug candidates, especially in routes involving bromoaryl building blocks for Suzuki or Ullmann-type reactions. Also utilized in the production of specialty chemicals where controlled substitution patterns on aromatic rings are required.

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