3-Chlorobenzyl bromide, 97%, Thermo Scientific Chemicals
3-Chlorobenzyl bromide, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Chlorobenzyl bromide, 97%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
10 g
50 g
Catalog number A15844.09
also known as A15844-09
Price (USD)/ Each
31.60
-
Add to cart
Quantity:
10 g
Request bulk or custom format
Price (USD)/ Each
31.60
Add to cart
3-Chlorobenzyl bromide, 97%, Thermo Scientific Chemicals
Catalog numberA15844.09
Price (USD)/ Each
31.60
-
Add to cart
Chemical Identifiers
CAS766-80-3
IUPAC Name1-(bromomethyl)-3-chlorobenzene
Molecular FormulaC7H6BrCl
InChI KeyLZIYAIRGDHSVED-UHFFFAOYSA-N
SMILESClC1=CC=CC(CBr)=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥96.0%
Refractive Index1.5860-1.5910 @ 20?C
3-Chlorobenzyl bromide was used in the synthesis of symmetrical and unsymmetrical benzyl thioethers. It was used as starting reagent during the synthesis of 1-(3-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole dihydrochloride.

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
3-Chlorobenzyl bromide was used in the synthesis of symmetrical and unsymmetrical benzyl thioethers. It was used as starting reagent during the synthesis of 1-(3-chlorobenzyl)-2-(pyrrolidin-1-ylmethyl)-1H-benzimidazole dihydrochloride.

Solubility
Decomposes in water.

Notes
Store at room temperature. Keep away from oxidizing agents.
RUO – Research Use Only
Leonardo Pisani.;Giovanni Muncipinto.; Teresa Fabiola Miscioscia.; Orazio Nicolotti.; Francesco Leonetti.; Marco Catto.; Carla Caccia.; Patricia Salvati.; Ramon Soto-Otero.; Estefania Mendez-Alvarez.; Celine Passeleu.; Angelo Carotti. Discovery of a Novel Class of Potent Coumarin Monoamine Oxidase B Inhibitors: Development and Biopharmacological Profiling of 7-[(3-Chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one Methanesulfonate (NW-1772) as a Highly Potent, Selective, Reversible, and Orally Active Monoamine Oxidase B InhibitorJ. Med. Chem. 2009, 52 (21), 6685-6706 .