产品名称
18-冠醚-6溶液, 1.0 M in THF
表单
liquid
环保替代产品特性
Catalysis
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sustainability
Greener Alternative Product
浓度
1.0 M in THF
密度
0.944 g/mL
环保替代产品分类
SMILES字符串
O1CCOCCOCCOCCOCCOCC1
InChI
1S/C12H24O6/c1-2-14-5-6-16-9-10-18-12-11-17-8-7-15-4-3-13-1/h1-12H2
InChI key
XEZNGIUYQVAUSS-UHFFFAOYSA-N
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
用于化学选择性还原熔融四氮唑和 NaBH4 以及氢氧化钾的相转移催化剂。
18-Crown-6 may be used to catalyze the N-alkylation of heterocyclic compounds and allylation of functionalized aldehydes.
Additive for greener etherification using KF-alumina.
Additive for greener etherification using KF-alumina.
Synthesis of diaryl ethers, diaryl thioethers, and diarylamines mediated by potassium fluoride-alumina and 18-crown-6
Synthesis of diaryl ethers, diaryl thioethers, and diarylamines mediated by potassium fluoride-alumina and 18-crown-6
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
靶器官
Respiratory system
补充剂危害
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
-2.0 °F
闪点(°C)
-18.88 °C
法规信息
新产品
此项目有
Synthesis, 3275-3275 (2006)
Phase-transfer alkylation of heterocycles in the presence of 18-crown-6 and potassium tert-butoxide.
Guida WC and Mathre DJ
The Journal of Organic Chemistry, 45(16), 3172-3176 (1980)
Preparation and purification of 18-crown-6 [1, 4, 7, 10, 13, 16-hexaoxacyclooctadecane].
Gokel GW, et al.
The Journal of Organic Chemistry, 39(16), 2445-2446 (1974)
Yu Chen et al.
Journal of the American Chemical Society, 134(4), 2313-2324 (2012-01-14)
Absolute 18-crown-6 (18C6) affinities of nine protonated peptidomimetic bases are determined using guided ion beam tandem mass spectrometry techniques. The bases (B) included in this work are mimics for the n-terminal amino group and the side chains of the basic
Tsutomu Yokozawa et al.
Macromolecular rapid communications, 32(11), 801-806 (2011-04-22)
(t)Bu(3) PPd(Ph)Br (1)-catalyzed Suzuki-Miyaura coupling polymerization of 2-(4-hexyl-5-iodo-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2) was investigated. Monomer 2 was polymerized with 1 at 0 °C in the presence of CsF and 18-crown-6 in THF containing a small amount of water to yield P3HT with a narrow
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