(2-Bromo-1,4-phenylene)dimethanol

≥95%

Reagent Code: #141767
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CAS Number 89980-92-7

science Other reagents with same CAS 89980-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.0599 g/mol
Formula C₈H₉BrO₂
badge Registry Numbers
MDL Number MFCD25968595
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) requiring brominated aromatic building blocks. Its dual hydroxymethyl groups allow for selective functionalization, enabling the construction of complex molecules in drug discovery. Also employed in the preparation of polymers and specialty resins where controlled reactivity and structural rigidity are needed. Commonly utilized in cross-coupling reactions such as Suzuki or Heck reactions to form biaryl structures in advanced organic synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,200.00
inventory 5g
10-20 days ฿12,800.00

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(2-Bromo-1,4-phenylene)dimethanol
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Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) requiring brominated aromatic building blocks. Its dual hydroxymethyl groups allow for selective functionalization, enabling the construction of complex molecules in drug discovery. Also employed in the preparation of polymers and specialty resins where controlled reactivity and structural rigidity are needed. Commonly utilized in cross-coupling re

Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) requiring brominated aromatic building blocks. Its dual hydroxymethyl groups allow for selective functionalization, enabling the construction of complex molecules in drug discovery. Also employed in the preparation of polymers and specialty resins where controlled reactivity and structural rigidity are needed. Commonly utilized in cross-coupling reactions such as Suzuki or Heck reactions to form biaryl structures in advanced organic synthesis.

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