1-Bromo-3-chlorobenzene
99%
Reagent
Code: #114767
Alias
1-bromo-3-chlorobenzene; 3-bromochlorobenzene, m-chlorobromobenzene, m-bromochlorobenzene, 3-chloro-1-bromobenzene
CAS Number
108-37-2
blur_circular Chemical Specifications
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Molecular Information
Weight
191.45 g/mol
Formula
C₆H₄BrCl
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Registry Numbers
EC Number
203-575-8
MDL Number
MFCD00000568
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Physical Properties
Melting Point
-21.5 °C
Boiling Point
196 °C(lit.)
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Storage & Handling
Density
1.63 g/mL at 25 °C(lit.)
Storage
room temperature
description Product Description
1-Bromo-3-chlorobenzene is widely used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its dual halogen substitution makes it a versatile building block for constructing more complex molecules. In the pharmaceutical industry, it is employed in the synthesis of active pharmaceutical ingredients (APIs) and fine chemicals. Additionally, it serves as a key reagent in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for creating carbon-carbon bonds in drug development. In agrochemicals, it is utilized to produce herbicides, pesticides, and fungicides, contributing to crop protection and agricultural productivity. Its stability and reactivity also make it valuable in material science for developing specialty polymers and dyes.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Specific Gravity (20/20°C) | 1.73-1.74 |
Purity (GC) | 99-100 |
Refractive Index (N20/D) | 1.575-1.578 |
Appearance | Colorless to light yellow liquid |
Infrared Spectrum | Conforms To Structure |
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1-Bromo-3-chlorobenzene
1-Bromo-3-chlorobenzene is widely used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its dual halogen substitution makes it a versatile building block for constructing more complex molecules. In the pharmaceutical industry, it is employed in the synthesis of active pharmaceutical ingredients (APIs) and fine chemicals. Additionally, it serves as a key reagent in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for creating carbon-carbon bonds in drug development. In agrochemicals, it is utilized to produce herbicides, pesticides, and fungicides, contributing to crop protection and agricultural productivity. Its stability and reactivity also make it valuable in material science for developing specialty polymers and dyes.
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