1,2-Benzenediol, 3-bromo-5-chloro-

≥95%

Reagent Code: #141682
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CAS Number 180995-18-0

science Other reagents with same CAS 180995-18-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.4518 g/mol
Formula C₆H₄BrClO₂
badge Registry Numbers
MDL Number MFCD23701700
thermostat Physical Properties
Boiling Point 273.3±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.952±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its halogenated phenolic structure. The compound serves in the development of antimicrobial agents and functionalized aromatic compounds. Its reactivity allows for further substitution reactions, making it valuable in organic synthesis and research laboratories. Also employed in the preparation of specialty polymers and antioxidants where halogen substitution enhances stability or biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,000.00
inventory 250mg
10-20 days ฿25,600.00
inventory 500mg
10-20 days ฿48,000.00
inventory 1g
10-20 days ฿67,200.00

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1,2-Benzenediol, 3-bromo-5-chloro-
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its halogenated phenolic structure. The compound serves in the development of antimicrobial agents and functionalized aromatic compounds. Its reactivity allows for further substitution reactions, making it valuable in organic synthesis and research laboratories. Also employed in the preparation of specialty polymers and antioxidants where halogen substitution enhances stability or biological activity.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its halogenated phenolic structure. The compound serves in the development of antimicrobial agents and functionalized aromatic compounds. Its reactivity allows for further substitution reactions, making it valuable in organic synthesis and research laboratories. Also employed in the preparation of specialty polymers and antioxidants where halogen substitution enhances stability or biological activity.

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