1-Chloro-3-fluorobenzene
95%
Reagent
Code: #114699
Alias
3-fluorochlorobenzene 1-fluoro-3-chlorobenzene m-fluorochlorobenzene m-chlorofluorobenzene
CAS Number
625-98-9
blur_circular Chemical Specifications
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Molecular Information
Weight
130.55 g/mol
Formula
C₆H₄ClF
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Registry Numbers
EC Number
210-919-0
MDL Number
MFCD00000569
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Physical Properties
Boiling Point
126-128 °C(lit.)
inventory_2
Storage & Handling
Density
1.219 g/mL at 25 °C(lit.)
Storage
room temperature
description Product Description
Widely used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It serves as a key building block in the production of active ingredients for drugs, particularly in the development of compounds with antibacterial and antifungal properties. Additionally, it is utilized in the manufacture of herbicides and pesticides, contributing to crop protection and agricultural productivity. Its role in organic synthesis extends to the creation of specialty chemicals and dyes, where its unique structure facilitates the introduction of functional groups in complex molecules. In research and development, it is employed as a reagent in chemical reactions to study reaction mechanisms and develop new synthetic pathways.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (%) | 94.5-100 |
Refractive Index (N20/D) | 1.492-1.497 |
Specific Gravity (20/20 °C) | 1.23-1.235 |
Appearance | Colorless To Light Yellow Liquid |
Infrared Spectrum | Conforms To Structure |
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1-Chloro-3-fluorobenzene
Widely used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It serves as a key building block in the production of active ingredients for drugs, particularly in the development of compounds with antibacterial and antifungal properties. Additionally, it is utilized in the manufacture of herbicides and pesticides, contributing to crop protection and agricultural productivity. Its role in organic synthesis extends to the creation of specialty chemicals and dyes, where its unique structure facilitates the introduction of functional groups in complex molecules. In research and development, it is employed as a reagent in chemical reactions to study reaction mechanisms and develop new synthetic pathways.
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