4-Bromo-3,5-dimethylphenol

90%

Reagent Code: #144234
label
Alias 4-Bromo-3,5-Dicinol 3,5-Dimethyl-4-Bromophenol
fingerprint
CAS Number 7463-51-6

science Other reagents with same CAS 7463-51-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.06 g/mol
Formula C₈H₉BrO
badge Registry Numbers
EC Number 231-255-8
MDL Number MFCD00002315
thermostat Physical Properties
Melting Point 113-115 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of reactive bromo and hydroxyl groups. Its structure allows for selective functionalization in organic reactions, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of biologically active compounds, including antimicrobial and anti-inflammatory agents. Its methyl-substituted phenol core contributes to enhanced lipophilicity and stability in final products.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 90-100
Appearance White crystal powder

shopping_cart Available Sizes & Pricing

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

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Bromo-3,5-dimethylphenol
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of reactive bromo and hydroxyl groups. Its structure allows for selective functionalization in organic reactions, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of biologically active compounds, including antimicrobial and anti-inflammatory agents. Its methyl-substit

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of reactive bromo and hydroxyl groups. Its structure allows for selective functionalization in organic reactions, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of biologically active compounds, including antimicrobial and anti-inflammatory agents. Its methyl-substituted phenol core contributes to enhanced lipophilicity and stability in final products.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...