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D57558

Sigma-Aldrich

2,6-Dichlorobenzonitrile

97%

Sinônimo(s):

Dichlobenil

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About This Item

Fórmula linear:
Cl2C6H3CN
Número CAS:
1194-65-6
Peso molecular:
172.01
Beilstein:
1909167
Número CE:
214-787-5
Número MDL:
MFCD00001781
Código UNSPSC:
12352100
ID de substância PubChem:
24893963
NACRES:
NA.22

Ensaio

97%

forma

powder

pf

143-146 °C (lit.)

cadeia de caracteres SMILES

Clc1cccc(Cl)c1C#N

InChI

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

chave InChI

YOYAIZYFCNQIRF-UHFFFAOYSA-N

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Aplicação

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.

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H312,H411

Classificações de perigo

Acute Tox. 4 Dermal - Aquatic Chronic 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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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)
Valeria Franceschini et al.
Stem cells (Dayton, Ohio), 27(4), 825-835 (2009-04-08)
The herbicide dichlobenil selectively causes necrosis of the dorsomedial part of olfactory neuroepithelium (NE) with permanent damage to the underlying mucosa, whereas the lateral part of the olfactory region and the nasal respiratory mucosa remain undamaged. We investigated here whether
L Peng et al.
Plant biology (Stuttgart, Germany), 15(2), 405-414 (2012-07-05)
Cellulose is the major component of plant cell walls and is an important source of industrial raw material. Although cellulose biosynthesis is one of the most important biochemical processes in plant biology, the regulatory mechanisms of cellulose synthesis are still
Fang Xie et al.
Toxicology and applied pharmacology, 272(3), 598-607 (2013-08-08)
We explored the mechanisms underlying the differential effects of two olfactory toxicants, the herbicide 2,6-dichlorobenzonitrile (DCBN) and the anti-thyroid drug methimazole (MMZ), on olfactory receptor neuron (ORN) regeneration in mouse olfactory epithelium (OE). DCBN, but not MMZ, induced inflammation-like pathological
Guang-Cai Chen et al.
Journal of hazardous materials, 188(1-3), 156-163 (2011-02-18)
The effect of lead on the adsorption of diuron and dichlobenil on multiwalled carbon nanotubes (MWCNTs) was investigated to explore the possible application of MWCNTs for removal of both herbicides from contaminated water. The adsorption of diuron and dichlobenil on
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