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经验公式(希尔记法):
C16H21O3P
化学文摘社编号:
分子量:
292.31
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
产品名称
1,3,5,7-四甲基-6-苯基-2,4,8-三氧-6-磷金刚烷, 97%
SMILES string
CC12CC3(C)OC(C)(CC(C)(O1)P3c4ccccc4)O2
InChI
1S/C16H21O3P/c1-13-10-15(3)19-14(2,17-13)11-16(4,18-13)20(15)12-8-6-5-7-9-12/h5-9H,10-11H2,1-4H3
InChI key
AVVSJWUWBATQBX-UHFFFAOYSA-N
assay
97%
form
solid
reaction suitability
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
reaction type: Cross Couplings
mp
106-111 °C
functional group
phosphine
Quality Level
Application
使用1,3,5,7-四甲基-6-苯基-2,4,8-三恶-6-磷酰金刚烷:
- 作为配体合成配合物用于氢甲酰化反应催化。
- 用于通过分子内环化羰基化反应催化二苯并b,f][1,4]]氧氮杂卓-11(10H)-酮和3-甲基-3,4-二氢香豆素的合成。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Diastereoselective and Branched-Aldehyde-Selective Tandem Hydroformylation-Hemiaminal Formation: Synthesis of Functionalized Piperidines and Amino Alcohols
Pittaway R, et al.
Organic Letters, 19(11), 2845-2848 (2017)
PdI2-Catalyzed Regioselective Cyclocarbonylation of 2-Allyl Phenols to Dihydrocoumarins
Ame?zquita-Valencia M and Alper H
Organic Letters, 16(22), 5827-5829 (2014)
Synthesis of Dibenzo [b, f][1, 4] oxazepin-11 (10 H)-ones via Intramolecular Cyclocarbonylation Reactions Using PdI2/Cytop 292 as the Catalytic System
Yang Q, et al.
The Journal of Organic Chemistry, 75(18), 6297-6299 (2010)
Phenylphosphatrioxa-adamantanes: bulky, robust, electron-poor ligands that give very efficient rhodium (I) hydroformylation catalysts
Baber RA, et al.
Dalton Transactions, 6, 1079-1085 (2005)
商品
Amines and phosphines in nucleophilic catalysis are discussed, addressing the air sensitivity of phosphines.
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