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Merck
CN

695459

1,3,5,7-四甲基-6-苯基-2,4,8-三氧-6-磷金刚烷

97%, solid

别名:

1,3,5,7-四甲基-8-苯基-2,4,6-三氧-8-磷酸三环 [3.3.1.1 3,7 ] 癸烷, meCgPPh

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关于此项目

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
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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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

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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