2-Bromo-4-chloro-1-nitrobenzene

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Reagent Code: #144319
label
Alias 2-Bromo-4-Chloro-1-Nitrobenzene
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CAS Number 63860-31-1

science Other reagents with same CAS 63860-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.45 g/mol
Formula C₆H₃BrClNO₂
badge Registry Numbers
MDL Number MFCD08437614
thermostat Physical Properties
Melting Point 49-50°C
Boiling Point 296.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Its functional groups allow for selective substitutions, making it valuable in the preparation of complex aromatic compounds. Commonly employed in the development of active ingredients in crop protection products and in the manufacture of certain therapeutic agents. Also utilized in research settings for constructing nitroaromatic scaffolds in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿780.00
inventory 10g
10-20 days ฿1,530.00
inventory 25g
10-20 days ฿3,770.00
inventory 100g
10-20 days ฿14,960.00
inventory 500g
10-20 days ฿65,010.00

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2-Bromo-4-chloro-1-nitrobenzene
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Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Its functional groups allow for selective substitutions, making it valuable in the preparation of complex aromatic compounds. Commonly employed in the development of active ingredients in crop protection products and in the manufacture of certain therapeutic agents. Also utilized in research settings for constructing nitroaromatic scaffolds in organic synthesis.

Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Its functional groups allow for selective substitutions, making it valuable in the preparation of complex aromatic compounds. Commonly employed in the development of active ingredients in crop protection products and in the manufacture of certain therapeutic agents. Also utilized in research settings for constructing nitroaromatic scaffolds in organic synthesis.

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