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Thermo Scientific Chemicals
3-Chlorobenzyl bromide, 97%
CAS: 766-80-3 | C7H6BrCl | 205.48 g/mol
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化學識別
CAS766-80-3
IUPAC Name1-(bromomethyl)-3-chlorobenzene
Molecular FormulaC7H6BrCl
InChI KeyLZIYAIRGDHSVED-UHFFFAOYSA-N
SMILESClC1=CC=CC(CBr)=C1
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規格
規格表
規格表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.
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 .