추천 제품
분석
≥99.0% (HPLC)
bp
298 °C (lit.)
mp
111-114 °C (lit.)
113-115 °C
SMILES string
C1c2ccccc2-c3ccccc13
InChI
1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2
InChI key
NIHNNTQXNPWCJQ-UHFFFAOYSA-N
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수량
λmax. 261 nm, log ε 4.28 (heptane)
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
303.8 °F - closed cup
Flash Point (°C)
151.0 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
New well-defined poly (2, 7-fluorene) derivatives: photoluminescence and base doping.
Ranger M, et al.
Macromolecules, 30(25), 7686-7691 (1997)
Qu Zhang et al.
Chemical communications (Cambridge, England), 51(50), 10182-10185 (2015-05-28)
Three amino-functionalized fluorene oligomers with different solubility were developed as cathode interfacial materials for inverted polymer solar cells (I-PSCs). By side chain design, we solved the interface layer erosion problem for I-PSCs, and the devices exhibit a power conversion efficiency
Priyanka Chaudhary et al.
Environmental monitoring and assessment, 187(6), 391-391 (2015-06-01)
Polyaromatic hydrocarbons (PAHs) utilizing bacteria were isolated from soils of seven sites of Mathura refinery, India. Twenty-six bacterial strains with different morphotypes were isolated. These strains were acclimatized to utilize a mixture of four polycyclic aromatic hydrocarbons, i.e., anthracene, fluorene
Spectroscopy and photochemistry of fluorene at a silica gel/air interface.
Barbas JT, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 109(3), 229-236 (1997)
Electroluminescent poly (fluorene-co-thiophene-S, S-dioxide): synthesis, characterisation and structure-property relationships.
Pasini M, et al.
Journal of Materials Chemistry, 13(4), 807-813 (2003)
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