추천 제품
제품 라인
ReagentPlus®
분석
≥99%
bp
243-245 °C (lit.)
mp
38-40 °C (lit.)
density
1.103 g/mL at 25 °C (lit.)
SMILES string
O=C1CCc2ccccc12
InChI
1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4H,5-6H2
InChI key
QNXSIUBBGPHDDE-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
1-Indanone can be used to synthesize:
It can also be used to build other indan-based systems like truxene, prekinamycin, indan-C60 and biindanylidenes.
- 11H-Indeno-[1,2-b]-quinolin-10-ylamine, a potential acetylcholinesterase inhibitor for the treatment of Alzheimer′s disease.
- CoumBARAC (coumarin fused biarylazacyclooctynone) for fluorogenic real-time imaging of azide-labeled biomolecules.
- Light emitting, organic semiconductors such as 4-pyrenyl-2-piperidin-1-yl-9H-fluorene-1-carbonitrile and bisindenoanthrazolines for organic light emitting diode (OLED) applications.
It can also be used to build other indan-based systems like truxene, prekinamycin, indan-C60 and biindanylidenes.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
233.0 °F - closed cup
Flash Point (°C)
111.67 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Indan-C 60: from a crystalline molecule to photovoltaic application.
Chemical Communications (Cambridge, England), 49(85), 9923-9925 (2013)
Highly efficient phosphorescent light-emitting diodes by using an electron-transport material with high electron affinity.
The Journal of Physical Chemistry C, 113(43), 18448-18450 (2009)
Acetylcholinesterase inhibitors for potential use in Alzheimer's disease: molecular modeling, synthesis and kinetic evaluation of 11H-indeno-[1, 2-b]-quinolin-10-ylamine derivatives.
Bioorganic & Medicinal Chemistry, 8(3), 497-506 (2000)
Donor-acceptor 9-uncapped fluorenes and fluorenones as stable blue light emitters.
Organic Letters, 11(6), 1289-1292 (2009)
Trisannulated benzene derivatives by acid catalyzed aldol cyclotrimerizations of cyclic ketones. Methodology development and mechanistic insight.
The Journal of Organic Chemistry, 72(9), 3412-3418 (2007)
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