721212
4-(4-(三丁基锡基)苯基)吗啉
别名:
4-(4-Tributylstannylphenyl)morpholine
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关于此项目
经验公式（希尔记法）:
C22H39NOSn
化学文摘社编号:
分子量:
452.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
InChI
1S/C10H12NO.3C4H9.Sn/c1-2-4-10(5-3-1)11-6-8-12-9-7-11;3*1-3-4-2;/h2-5H,6-9H2;3*1,3-4H2,2H3;
SMILES string
CCCC[Sn](CCCC)(CCCC)c1ccc(cc1)N2CCOCC2
InChI key
VIPDIXBRZHVCRF-UHFFFAOYSA-N
form
liquid
refractive index
n20/D 1.541
density
1.175 g/L at 25 °C
Application
4-(4-(Tributylstannyl)phenyl)morpholine is an organotin compound that can be used as a reactant in:
- Palladium-catalyzed Stille cross-coupling reaction.
- Regio and diastereoselective preparation of (perfluoroalkyl)arylethenes via Pd-catalyzed three-component iodoperfluoroalkylation and Stille coupling reaction.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Palladium-Catalyzed Carboperfluoroalkylation of Alkynes with Fluoroalkyl Iodides and Arylstannanes
Upadhyay NS and Chaladaj W
advanced synthesis and catalysis, 87(1), 91-113 (2019)
Palladium-Catalyzed Carboperfluoroalkylation of Alkynes with Fluoroalkyl Iodides and Arylstannanes
Upadhyay NS and Chaladaj W
Advanced Synthesis & Catalysis, 87(1), 91-113 (2019)
Preparation of a diverse purine-scaffold library via one-step palladium catalyzed cross-coupling
Taldone T, et al.
Heterocycles, 87(1), 91-113 (2013)
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