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Key Documents

D57558

Sigma-Aldrich

2,6-Dichlorobenzonitrile

97%

Synonym(s):

Dichlobenil

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About This Item

Linear Formula:
Cl2C6H3CN
CAS Number:
Molecular Weight:
172.01
Beilstein:
1909167
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

powder

mp

143-146 °C (lit.)

SMILES string

Clc1cccc(Cl)c1C#N

InChI

1S/C7H3Cl2N/c8-6-2-1-3-7(9)5(6)4-10/h1-3H

InChI key

YOYAIZYFCNQIRF-UHFFFAOYSA-N

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Application

2,6-Dichlorobenzonitrile can be used as a starting material to synthesize:
  • 2,6-Dichlorobenzaldehyde using lithium N, N′-dimethylethylenediaminoaluminum hydride as a reducing agent.
  • 5-(2,6-Dichlorophenyl)-2H-tetrazole via gold-catalyzed nucleophilic (3 + 2) cycloaddition reaction with sodium azide.
  • 2,6-Dichlorobenzamide via hydrolysis using potassium tert-butoxide as a catalyst.
  • Chloro-aminoindazole by reacting with hydrazine monohydrate.
  • 2,6-Dichlorobenzenecarboselenoamide by treating with Woollins′ reagent.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Aquatic Chronic 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of primary arylselenoamides by reaction of aryl nitriles with Woollins' reagent
Hua Guoxiong, et al.
Organic Letters, 8(23), 5251-5254 (2006)
The discovery and development of a safe, practical synthesis of ABT-869
Kruger AW, et al.
Organic Process Research & Development, 13(6), 1419-1425 (2009)
Synthetic application of gold nanoparticles and auric chloride for the synthesis of 5-substituted 1 H-tetrazoles
Kumar S, et al.
Royal Society of Chemistry Advances, 5(28), 21651-21658 (2015)
Transition-metal-free hydration of nitriles using potassium tert-butoxide under anhydrous conditions
Midya GC, et al.
The Journal of Organic Chemistry, 80(8), 4148-4151 (2015)
Selective conversion of aromatic nitriles to aldehydes by lithium N, N'-dimethylethylenediaminoaluminum hydride
Cha Jin-Soon, et al.
Bulletin of the Korean Chemical Society,, 23(12), 1697-1698 (2002)

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