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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
产品名称
2,6-二氯苯腈, 97%
InChI key
YOYAIZYFCNQIRF-UHFFFAOYSA-N
InChI
1S/C7H3Cl2N/c8-6-2-1-3-7(9)5(6)4-10/h1-3H
SMILES string
Clc1cccc(Cl)c1C#N
assay
97%
form
powder
mp
143-146 °C (lit.)
Quality Level
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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.
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
此项目有
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)
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)
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)
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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