56849
芴
certified reference material, TraceCERT®
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经验公式（希尔记法）:
C13H10
化学文摘社编号:
分子量:
166.22
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
201-695-5
Beilstein/REAXYS Number:
1363491
MDL number:
InChI
1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2
SMILES string
C1c2ccccc2-c3ccccc13
InChI key
NIHNNTQXNPWCJQ-UHFFFAOYSA-N
grade
certified reference material, TraceCERT®
product line
TraceCERT®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
298 °C (lit.)
mp
111-114 °C (lit.)
application(s)
environmental
format
neat
Quality Level
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General description
This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Legal Information
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
303.8 °F - closed cup
flash_point_c
151.0 °C - closed cup
Laser-induced carbene-carbene rearrangement in solution: the diphenylcarbene-fluorene rearrangement.
Michèle J Régimbald-Krnel et al.
The Journal of organic chemistry, 78(17), 8789-8795 (2013-08-15)
Diphenylcarbene (DPC) generated by high-intensity laser photolysis of diphenyldiazomethane rearranges to fluorene (FL) by two distinct mechanisms as revealed by methyl-group labeling. Thus, excimer laser irradiation of p,p'-dimethyldiphenyldiazomethane generates 3,6-dimethylfluorene (3,6-DMF) and 2,7-dimethylfluorene (2,7-DMF), which were identified by fluorescence measurements
S A Schmid et al.
Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 370(1972), 3787-3801 (2012-07-04)
We have investigated the energy transfer dynamics in a supramolecular linear polymer chain comprising oligofluorene (OF) energy donor units linked by quadruple hydrogen-bonding groups, and oligophenylene (OPV) chain ends that act as energy acceptors. Using femtosecond spectroscopy, we followed the
Pierre Lovera et al.
Journal of nanoscience and nanotechnology, 13(7), 5194-5202 (2013-08-02)
Organic nanowires based on a fluorene homopolymer and a copolymer, i.e., poly(9,9-dioctylfluorene), F8, and poly(9,9-dioctylfluorene-co-benzothiadiazole), F8BT, respectively, were synthesised by solution assisted wetting of porous anodic alumina templates. Nanowires ranged between 3 microm and 50 microm in length, and were
Atul Kumar Dwivedi et al.
ACS applied materials & interfaces, 4(11), 6371-6377 (2012-11-02)
Because of the toxicity caused by the heme redox-active iron proteins, their elevated levels, localization, and accumulation in the brain, many forms of neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease, occur as a result of which
Shuying Ma et al.
Chemical communications (Cambridge, England), 48(97), 11847-11849 (2012-11-02)
A novel 3D donor material (SF8TBT) based on spiro-fluorene has been developed. Compared with the corresponding 1D linear molecule, the OPVs of this 3D donor exhibited power conversion efficiencies of 4.82%, much higher than that of 1D small molecules (1.69%).
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