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质量水平
方案
97%
表单
powder
mp
143-146 °C (lit.)
SMILES字符串
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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应用
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.
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Dermal - Aquatic Chronic 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
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)
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)
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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