(4-(Bromomethyl)phenyl)methanol

97%

  • Product Code: 121909
  CAS:    71831-21-5
Molecular Weight: 201.06 g./mol Molecular Formula: C₈H₉BrO
EC Number: MDL Number: MFCD08275218
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: (4-(Bromomethyl)phenyl)methanol is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its structure, featuring both a bromomethyl and a hydroxymethyl group, makes it a versatile building block for constructing more complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) and in the development of compounds with potential therapeutic properties. Additionally, it can be utilized in the preparation of polymers and resins, where its reactive sites allow for further functionalization. In research, it serves as a key reagent in the study of chemical reactions and the development of new synthetic methodologies.
Product Specification:
Test Specification
Appearance White To Yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿350.00
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0.250 10-20 days ฿560.00
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1.000 10-20 days ฿1,800.00
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5.000 10-20 days ฿8,550.00
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(4-(Bromomethyl)phenyl)methanol
(4-(Bromomethyl)phenyl)methanol is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its structure, featuring both a bromomethyl and a hydroxymethyl group, makes it a versatile building block for constructing more complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) and in the development of compounds with potential therapeutic properties. Additionally, it can be utilized in the preparation of polymers and resins, where its reactive sites allow for further functionalization. In research, it serves as a key reagent in the study of chemical reactions and the development of new synthetic methodologies.
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