추천 제품
Quality Level
제품 라인
ReagentPlus®
분석
99%
bp
245-248 °C (lit.)
mp
114-116 °C (lit.)
SMILES string
[H]C(=O)c1ccc(cc1)C([H])=O
InChI
1S/C8H6O2/c9-5-7-1-2-8(6-10)4-3-7/h1-6H
InChI key
KUCOHFSKRZZVRO-UHFFFAOYSA-N
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애플리케이션
Terephthalaldehyde can be used as a starting material for:
- The synthesis of fused bis-benzoquinoline derivatives on reacting with arylamines and cyclic ketones through one pot three component reaction.
- The photochemical synthesis of 5,10-disubstituted[5]helicenes by reacting with benzyl cyanide via Knoevenagel reaction.
- The synthesis of a nitronyl nitroxide (NIT) radical with a pyrimidiniumolate unit, which are useful precursors for building molecular magnets.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
이미 열람한 고객
Facile photochemical synthesis of 5, 10-disubstituted [5] Helicenes by removing molecular orbital degeneracy
Organic Letters, 16(9), 2502-2505 (2014)
Camphorsulfonic acid catalyzed one-pot three-component reaction for the synthesis of fused quinoline and benzoquinoline derivatives
The Journal of Organic Chemistry, 82(23), 12416-12429 (2017)
Synthesis of dipolar nitronyl nitroxides
Organic Letters, 2(15), 2269-2270 (2000)
Journal of the American Chemical Society, 137(27), 8819-8828 (2015-06-23)
We report the systematic characterization of anisotropic, π-conjugated oligophenyleneimine (OPI) films synthesized using stepwise imine condensation, or "click" chemistry. Film synthesis began with a self-assembled monolayer (SAM) of 4-formylthiophenol or 4-aminothiophenol on Au, followed by repetitive, alternate addition of terephthalaldehyde
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