523380
4-[(Trimethylsilyl)ethynyl]benzaldehyde
97%
동의어(들):
4-(Trimethylsilylethynyl)benzaldehyde, 4-[2-(Trimethylsilyl)ethynyl]benzaldehyde, p-[(Trimethylsilyl)ethynyl]benzaldehyde
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모든 사진(2)
About This Item
Linear Formula:
(CH3)3SiC≡CC6H4CHO
CAS Number:
Molecular Weight:
202.32
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
mp
66-70 °C (lit.)
작용기
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
일반 설명
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.
애플리케이션
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
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
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)
Linear porphyrin dimers with fluorenyl arms linked by an ethynyl bridge.
Merhi A, et al.
Tetrahedron, 69(34), 7112-7124 (2013)
Synthesis of covalently bonded nanostructure from two porphyrin molecular wires leading to a molecular tube.
Ishida T, et al.
Tetrahedron Letters, 47(30), 5265-5268 (2006)
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)
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