523380
4-[(三甲基硅基)乙炔基]苯甲醛
97%
别名:
4-(Trimethylsilylethynyl)benzaldehyde, 4-[2-(Trimethylsilyl)ethynyl]benzaldehyde, p-[(Trimethylsilyl)ethynyl]benzaldehyde
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关于此项目
线性分子式:
(CH3)3SiC≡CC6H4CHO
化学文摘社编号:
分子量:
202.32
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Quality Segment
assay
97%
mp
66-70 °C (lit.)
functional group
aldehyde
SMILES string
C[Si](C)(C)C#Cc1ccc(C=O)cc1
InChI
1S/C12H14OSi/c1-14(2,3)9-8-11-4-6-12(10-13)7-5-11/h4-7,10H,1-3H3
InChI key
UZQDUXAJFTWMDT-UHFFFAOYSA-N
General description
4-[(Trimethylsilyl)ethynyl]benzaldehyde can be synthesized by reacting 4-bromobenzaldehyde and triphenylphosphine in anhydrous triethylamine with ethynyltrimethylsilane and then with palladium(II) acetate under argon. It can also be prepared by Sonogashira coupling reaction between 4-bromobenzaldehyde and (trimethylsilyl) ethynyl.
Application
4-[(Trimethylsilyl)ethynyl]benzaldehyde may be used in the preparation of the following:
- 4,4,5,5-tetramethyl-2-{4-[(trimethylsilyl)ethynyl]phenyl}imidazolidine-1,3-diol
- 5,10,15-triphenyl-20-{4-[2-(trimethylsilyl)ethynyl]phenyl}porphyrin
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
On the potential of porphyrin-spiked triarylamine stars for bulk heterojunction solar cells.
Kengthanomma T, et al.
Journal of Material Chemistry A, 1(35), 10524-10531 (2013)
Cascade Reactions of Me3Si-Substituted Imidazolidine-1, 3-Diols with PbO2, Including Oxidation of the Corresponding Diol and Subsequent Elimination of the Trimethylsilyl Fragment.
Tretyakov E, et al.
European Journal of Organic Chemistry, 2007(22), 3639-3647 (2007)
Facile synthesis of ethynylated benzoic acid derivatives and aromatic compounds via ethynyltrimethylsilane.
Austin WB, et al.
The Journal of Organic Chemistry, 46(11), 2280-2286 (1981)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 523380-5G | 04061832548050 |