1-(2-Bromo-6-hydroxyphenyl)ethanone

97%

Reagent Code: #148542
fingerprint
CAS Number 55736-69-1

science Other reagents with same CAS 55736-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.04 g/mol
Formula C₈H₇BrO₂
badge Registry Numbers
MDL Number MFCD13193630
thermostat Physical Properties
Boiling Point 276.777°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its functional groups—bromine and hydroxyl—allow for selective substitutions and coupling reactions, making it valuable in constructing complex aromatic compounds. Commonly employed in the development of analgesics and anti-inflammatory agents due to its reactivity in forming carbon-carbon and carbon-heteroatom bonds. Also utilized in the synthesis of dyes and UV stabilizers where phenolic structures are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,780.00
1g
10-20 days ฿4,520.00
5g
10-20 days ฿16,720.00
10g
10-20 days ฿32,480.00
1-(2-Bromo-6-hydroxyphenyl)ethanone
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its functional groups—bromine and hydroxyl—allow for selective substitutions and coupling reactions, making it valuable in constructing complex aromatic compounds. Commonly employed in the development of analgesics and anti-inflammatory agents due to its reactivity in forming carbon-carbon and carbon-heteroatom bonds. Also utilized in the synthesis of dyes and UV stabilizers where phenolic

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its functional groups—bromine and hydroxyl—allow for selective substitutions and coupling reactions, making it valuable in constructing complex aromatic compounds. Commonly employed in the development of analgesics and anti-inflammatory agents due to its reactivity in forming carbon-carbon and carbon-heteroatom bonds. Also utilized in the synthesis of dyes and UV stabilizers where phenolic structures are required.

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...