2,3-Dichlorobenzonitrile, 98%
2,3-Dichlorobenzonitrile, 98%
2,3-Dichlorobenzonitrile, 98%
2,3-Dichlorobenzonitrile, 98%
Thermo Scientific Chemicals

2,3-Dichlorobenzonitrile, 98%

CAS: 6574-97-6 | C7H3Cl2N | 172.008 g/mol
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25 g
Catalog number A14809.14
also known as A14809-14
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25 g
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Price (USD)
385.65
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Online exclusive
Ends: 30-Jun-2026
454.00
Save 68.35 (15%)
Each
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Chemical Identifiers
CAS6574-97-6
IUPAC Name2,3-dichlorobenzonitrile
Molecular FormulaC7H3Cl2N
InChI KeyOHDYZVVLNPXKDX-UHFFFAOYSA-N
SMILESClC1=CC=CC(C#N)=C1Cl
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SpecificationsSpecification SheetSpecification Sheet
FormPowder
Assay (GC)≥97.5%
Melting Point (clear melt)59.5-65.5?C
Appearance (Color)White
2,3-Dichlorobenzonitrile, is used as a reactant involved in nucleophilic aromatic fluorination, reactions with magnesium amides for synthesis of carboxamides, Suzuki-Miyaura coupling reactions. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dye stuff.

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
2,3-Dichlorobenzonitrile, is used as a reactant involved in nucleophilic aromatic fluorination, reactions with magnesium amides for synthesis of carboxamides, Suzuki-Miyaura coupling reactions. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dye stuff.

Solubility
It is miscible with water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Lendon N. Pridgen .; Lewis B. Killmer .; R. Lee Webb. Oxazolines. 2. 2-Substituted 2-oxazolines as synthons for N-(.beta.-hydroxyethyl)arylalkylamines, intermediates in a synthesis of 1,2,3,4-tetrahydroisoquinolines and 2,3,4,5-tetrahydro-1H-3-benzazepines. J. Org. Chem. 1982, 47, (11), 1985-1989.
  2. Tsuneo Imamoto.; et.al. Carbon-carbon bond-forming reactions using cerium metal or organocerium(III) reagents. J. Org. Chem. 1984, 49, (21), 3904-3912.