所有图片(2)
About This Item
经验公式（希尔记法）:
C9H17ClN2
CAS号:
分子量:
188.70
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
97%
表单
solid
反应适用性
reagent type: catalyst
环保替代产品特性
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
182-186 °C
环保替代产品分类
SMILES字符串
[Cl-].CC(C)n1cc[n+](c1)C(C)C
InChI
1S/C9H17N2.ClH/c1-8(2)10-5-6-11(7-10)9(3)4;/h5-9H,1-4H3;1H/q+1;/p-1
InChI key
DOFXKPAOJLLPII-UHFFFAOYSA-M
相关类别
一般描述
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
应用
1,3-Diisopropylimidazolium chloride may be used to prepare:
- 1,3-Diisopropylimidazole-2-thione by reacting with sulfur in the presence of potassium carbonate.
- (C9H7)NiCl(1,3-diisopropylimidazol-2- ylidene) by reacting with bis-indenyl nickel-(II).
- Ruthenium N-heterocyclic carbene complexes, which are efficient catalysts for the amidation of primary alcohols and amines.
Ligand for ruthenium-catalyzed greener amide bond formation by dehydrogenative coupling of amines and alcohols.
Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen
Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
A dinuclear Bi (III) complex of a 1, 3-disubstituted imidazole-2-thione and its use as a transmetallation agent toward Pd (II).
Jagenbrein M, et al.
Journal of Organometallic Chemistry, 796, 11-16 (2015)
Amide Synthesis from Alcohols and Amines Catalyzed by Ruthenium N-Heterocyclic Carbene Complexes.
Dam JH, et al.
Chemistry?A European Journal , 16(23), 6820-6827 (2010)
Indenylnickel (II) N-heterocyclic carbene complexes: Synthesis via indene elimination and catalytic activity for ethylene dimerization.
Sun HM, et al.
Organometallics, 24(2), 331-334 (2005)
Chen C and Hong SH.
Organic & Biomolecular Chemistry, 9(1), 20-26 (2011)
实验方案
乙炔化学一直是并且仍然是分子科学的重要组成部分。它的潜力和广泛的应用从有机合成到材料科学再到生物有机化学。一些例子是烯二炔（DNA切割剂），“点击化学”工具和构建块。 因此，它引发了对高效合成炔烃的需求。
Acetylene chemistry's versatile applications from organic synthesis to bioorganic chemistry demand efficient synthesis methods.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
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