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Merck
CN

D57558

2,6-二氯苯腈

97%

别名:

敌草腈

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关于此项目

线性分子式:
Cl2C6H3CN
化学文摘社编号:
分子量:
172.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-787-5
Beilstein/REAXYS Number:
1909167
MDL number:
Assay:
97%
Form:
powder
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Quality Level

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

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

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Dermal - Aquatic Chronic 2

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

农药列管产品

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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)



全球贸易项目编号

货号GTIN
D57558-25G04061832108902