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质量水平
方案
98%
表单
liquid
折射率
n20/D 1.459 (lit.)
沸点
72-73 °C/6 mmHg (lit.)
密度
0.883 g/mL at 25 °C (lit.)
官能团
ketone
SMILES字符串
CC(C)(C)C(=O)CC(=O)C(C)(C)C
InChI
1S/C11H20O2/c1-10(2,3)8(12)7-9(13)11(4,5)6/h7H2,1-6H3
InChI key
YRAJNWYBUCUFBD-UHFFFAOYSA-N
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一般描述
2,2,6,6-四甲基-3,5-庚二酮是一种双齿配体,用于与镧系离子合成稳定的配合物。
2,2,6,6-四甲基-3,5-庚二酮是一种稳定的无水试剂。它经历氧加成和碳加成。在各种反应中,它作为金属催化剂的空气稳定配体发挥作用。此外,它还可用作杂环的底物。
2,2,6,6-四甲基-3,5-庚二酮是一种稳定的无水试剂。它经历氧加成和碳加成。在各种反应中,它作为金属催化剂的空气稳定配体发挥作用。此外,它还可用作杂环的底物。
应用
2,2,6,6-四甲基-3,5-庚二酮用于合成α-芳基-β-二酮和二氰胺-苯桥二钌络合物。
2,2,6,6-四甲基-3,5-二庚酮,以在在合成橙色发光铱(III)络合物中用作辅助配体。
2,2,6,6-四甲基-3,5-二庚酮,以在在合成橙色发光铱(III)络合物中用作辅助配体。
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
152.6 °F - closed cup
闪点(°C)
67 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Thermochemistry of 2, 2, 6, 6-tetramethyl-3, 5-heptanedione chelates of lanthanide group elements
Santos Jr, et al.
Polyhedron, 18, 969-977 (1999)
Synthesis and characterization of phenylpyridine derivative containing an imide functional group on an iridium (III) complex for solution-processable orange-phosphorescent organic light-emitting diodes
Hwang J, et al.
Dyes and Pigments, 121, 73-78 (2015)
Solvent extraction of some lanthanides with 2, 2, 6, 6-tetramethyl-3, 5-heptanedione
Sweet TR and Parlett HW
Analytical Chemistry, 40(12), 1885-1888 (1968)
2, 2, 6, 6-Tetramethyl-3, 5-heptanedione
Jurica EA
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Muriel Fabre et al.
Inorganic chemistry, 45(23), 9332-9345 (2006-11-07)
The dicyanamidobenzene-bridge diruthenium complex [{Ru(tpy)(thd)}(2)(mu-dicyd)][PF(6)] ([3][PF(6)]) (dicyd = 1,4-dicyanamidobenzene, tpy = 2,2':6',2' '-terpyridine, thd = 2,2,6,6-tetramethyl-3,5-heptanedione) and its mononuclear counterpart [Ru(tpy)(thd)(Ipcyd)] (2) [Ipcyd = 4-iodophenylcyanamide anion (Ipcyd(-))] were synthesized and fully characterized. Cyclic voltammetry of 3 showed the presence of
商品
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
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