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Thermo Scientific Chemicals
4-Bromobenzyl chloride, 97%
CAS: 589-17-3 | C7H6BrCl | 205.48 g/mol
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Catalog number L11486.06
also known as L11486-06
Price (USD)
45.65
Special offer
Online exclusive
Ends: 30-Jun-2026
53.20Save 7.55 (14%)
Each
Quantity:
5 g
Price (USD)
45.65
Special offer
Online exclusive
Ends: 30-Jun-2026
53.20Save 7.55 (14%)
Each
Chemical Identifiers
CAS589-17-3
IUPAC Name1-bromo-4-(chloromethyl)benzene
Molecular FormulaC7H6BrCl
InChI KeyBSIIGUGKOPPTPZ-UHFFFAOYSA-N
SMILESClCC1=CC=C(Br)C=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to gray
FormCrystals or powder or crystalline powder or fused solid or flakes
Melting Point (clear melt)34.0-44.0?C
Identification (FTIR)Conforms
Assay (GC)≥96.0%
4-Bromobenzyl chloride is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-Bromobenzyl chloride is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.
Solubility
Insoluble in water.
Notes
Keep container tightly closed. Store in cool, dry conditions in well sealed containers. Incompatible with strong bases and strong oxidizing agents.
4-Bromobenzyl chloride is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.
Solubility
Insoluble in water.
Notes
Keep container tightly closed. Store in cool, dry conditions in well sealed containers. Incompatible with strong bases and strong oxidizing agents.
RUO – Research Use Only
Nicolas Henry.; Cécile Enguehard-Gueiffier.; Isabelle Thery.; Alain Gueiffier. One-Pot Dual Substitutions of Bromobenzyl Chloride, 2-Chloromethyl-6-halogenoimidazo[1,2-a]pyridine and -[1,2-b]pyridazine by Suzuki-Miyaura Cross-Coupling Reactions. European Journal of Organic Chemistry. 2008, 2008 (28), 4824-4827.